This is a table of type bigram and their frequencies. Use it to search & browse the list to learn more about your study carrel.
bigram | frequency |
---|---|
patients will | 155 |
informed consent | 154 |
data will | 144 |
mechanical ventilation | 143 |
sample size | 140 |
adverse events | 139 |
study will | 138 |
controlled trial | 128 |
control group | 111 |
clinical trial | 110 |
acute respiratory | 110 |
will also | 106 |
will receive | 101 |
additional file | 97 |
study protocol | 94 |
lung injury | 91 |
primary outcome | 89 |
respiratory distress | 87 |
adverse event | 85 |
participants will | 84 |
randomized controlled | 82 |
intensive care | 81 |
clinical trials | 81 |
trial will | 80 |
distress syndrome | 77 |
full protocol | 76 |
group will | 75 |
study intervention | 75 |
data collection | 74 |
ethics committee | 72 |
mg kg | 70 |
analyses will | 70 |
critically ill | 69 |
exclusion criteria | 69 |
respiratory failure | 68 |
study drug | 64 |
within days | 63 |
serious adverse | 61 |
will include | 61 |
analysis will | 61 |
clinical practice | 58 |
randomised controlled | 58 |
trial registration | 58 |
ill patients | 57 |
primary endpoint | 57 |
samples will | 57 |
acute lung | 56 |
secondary outcomes | 55 |
blood pressure | 54 |
inclusion criteria | 51 |
twice daily | 50 |
statistical analysis | 50 |
consent form | 48 |
clinical study | 47 |
systematic review | 46 |
care unit | 46 |
treatment group | 44 |
investigator will | 44 |
ravulizumab bsc | 44 |
pao fio | 44 |
cord uid | 42 |
doc id | 42 |
trials doi | 42 |
pilot rct | 42 |
interim analysis | 42 |
principal investigator | 42 |
protocol amendment | 41 |
two groups | 40 |
icu patients | 39 |
organ failure | 39 |
intervention group | 38 |
consent will | 37 |
risk factors | 37 |
trial design | 37 |
case report | 37 |
public health | 37 |
study team | 37 |
data protection | 36 |
breast cancer | 36 |
chronic obstructive | 36 |
will use | 36 |
pulmonary disease | 36 |
investigators will | 36 |
critical care | 36 |
study center | 36 |
outcomes will | 35 |
invasive mechanical | 35 |
lung function | 35 |
analysis plan | 35 |
clinical improvement | 35 |
patients randomized | 35 |
indigenous infants | 34 |
airway pressure | 34 |
within hours | 34 |
obstructive pulmonary | 34 |
will provide | 34 |
randomization will | 34 |
medical records | 32 |
will take | 32 |
steering committee | 32 |
air pollution | 31 |
respiratory syndrome | 31 |
severe acute | 31 |
dornase alfa | 31 |
dans le | 31 |
protocol version | 31 |
information will | 30 |
missing data | 30 |
first days | 30 |
bsc alone | 30 |
blood gas | 30 |
venous thromboembolism | 30 |
clinical research | 30 |
study design | 29 |
hospitalized patients | 29 |
least one | 29 |
supplemental oxygen | 29 |
icu admission | 29 |
severe covid | 28 |
institutional affiliations | 28 |
per year | 28 |
hospital admission | 28 |
oxygen saturation | 28 |
legally acceptable | 28 |
physical activity | 28 |
report form | 28 |
events will | 28 |
springer nature | 28 |
trial date | 28 |
published maps | 28 |
remains neutral | 28 |
jurisdictional claims | 28 |
patients admitted | 28 |
patient will | 28 |
hypoxic respiratory | 28 |
results will | 28 |
nature remains | 28 |
vector control | 27 |
treatment will | 27 |
side effects | 27 |
clinical outcomes | 27 |
arterial blood | 27 |
blood samples | 27 |
study participants | 26 |
study medication | 26 |
coronavirus disease | 26 |
preterm infants | 26 |
le promoteur | 26 |
healthcare workers | 26 |
gum arabic | 26 |
usual care | 26 |
acceptable representative | 26 |
gut microbiota | 26 |
cure rct | 26 |
lopinavir ritonavir | 26 |
day mortality | 26 |
bubonic plague | 26 |
vestibular function | 26 |
study data | 26 |
primary efficacy | 26 |
les patients | 25 |
cytokine storm | 25 |
treatment groups | 25 |
clinical data | 25 |
research team | 25 |
monitoring committee | 25 |
take place | 25 |
treating physician | 25 |
new zealand | 25 |
trauma patients | 25 |
data analysis | 25 |
copd exacerbation | 24 |
acute hypoxic | 24 |
hearing loss | 24 |
study site | 24 |
hospital discharge | 24 |
written informed | 24 |
randomized clinical | 23 |
eligibility criteria | 23 |
mechanically ventilated | 23 |
university hospital | 23 |
nasal cpap | 23 |
study period | 23 |
note springer | 23 |
participating centers | 23 |
medical patients | 23 |
investigator must | 23 |
blood sample | 23 |
competing interests | 23 |
respiratory symptoms | 22 |
logistic regression | 22 |
icu pilot | 22 |
main outcomes | 22 |
secondary endpoints | 22 |
ward pilot | 22 |
trials website | 22 |
expediting dissemination | 22 |
data management | 22 |
respiratory rate | 22 |
ordinal scale | 22 |
letter serves | 22 |
adult patients | 22 |
behaviour change | 22 |
key elements | 22 |
physical examination | 22 |
familiar formatting | 22 |
outcome measures | 22 |
randomly assigned | 22 |
enoxaparin sodium | 22 |
health organization | 22 |
pneumonic plague | 22 |
kfsh rc | 21 |
lung disease | 21 |
site staff | 21 |
eligible patients | 21 |
cohort study | 21 |
size calculation | 21 |
data monitoring | 21 |
good clinical | 21 |
intervention period | 21 |
parallel group | 21 |
supplementary information | 21 |
source data | 21 |
sensorineural hearing | 21 |
asthma exacerbations | 21 |
crf ecrf | 21 |
patients per | 21 |
hiruz ctu | 21 |
live home | 21 |
controlled trials | 21 |
primary analysis | 21 |
free days | 21 |
cytokine release | 21 |
positive end | 21 |
world health | 21 |
clinical studies | 21 |
trial status | 21 |
yes vs | 20 |
patient information | 20 |
study participation | 20 |
inspired oxygen | 20 |
myocardial infarction | 20 |
pregnancy test | 20 |
supportive care | 20 |
mortality rate | 20 |
main trial | 20 |
principal investigators | 20 |
source documents | 20 |
primary outcomes | 20 |
experimental group | 20 |
study physician | 20 |
expiratory pressure | 20 |
infected patients | 20 |
written consent | 20 |
novel coronavirus | 20 |
vital signs | 19 |
oxygen therapy | 19 |
authors declare | 19 |
efficacy outcome | 19 |
gas exchange | 19 |
ketamine infusion | 19 |
intervention will | 19 |
severe pneumonia | 19 |
groups will | 19 |
confidence interval | 19 |
information accompanies | 19 |
performed using | 19 |
clinically significant | 19 |
sodium chloride | 19 |
heart failure | 19 |
variables will | 19 |
complement activation | 19 |
indoor residual | 19 |
standard deviation | 19 |
per group | 19 |
residual spraying | 19 |
function tests | 19 |
traitement par | 19 |
balance main | 18 |
patients aged | 18 |
final manuscript | 18 |
release syndrome | 18 |
study drugs | 18 |
recruitment manoeuvre | 18 |
female patients | 18 |
high risk | 18 |
significance level | 18 |
medical history | 18 |
staff will | 18 |
safety monitoring | 18 |
structured summary | 18 |
study treatment | 18 |
par le | 18 |
heart rate | 18 |
flow nasal | 18 |
sofa score | 18 |
coordinating investigator | 18 |
analyzed using | 18 |
randomized trial | 18 |
causal relationship | 18 |
hypertension control | 17 |
major bleeding | 17 |
screening period | 17 |
untoward medical | 17 |
medicinal product | 17 |
outcome will | 17 |
interim analyses | 17 |
sudden sensorineural | 17 |
budesonide formoterol | 17 |
will occur | 17 |
rank test | 17 |
corresponding author | 17 |
protocol amendments | 17 |
subject will | 17 |
adverse reaction | 17 |
cancer survivors | 17 |
mg ml | 17 |
phase ii | 17 |
type i | 17 |
positive airway | 17 |
auxiliary nurses | 17 |
nasal obstruction | 17 |
cystic fibrosis | 17 |
personal data | 16 |
monitoring board | 16 |
electronic data | 16 |
statistical methods | 16 |
research ethics | 16 |
patients may | 16 |
patients enrolled | 16 |
icu stay | 16 |
dans les | 16 |
arm will | 16 |
effect size | 16 |
clavulanic acid | 16 |
respiratory tract | 16 |
study procedures | 16 |
will continue | 16 |
medical management | 16 |
ventilated patients | 16 |
medical occurrence | 16 |
severe hypoxaemia | 16 |
may also | 16 |
respiratory illness | 16 |
renal function | 16 |
standard protocol | 16 |
control arm | 16 |
information sheet | 16 |
primary evaluation | 16 |
day will | 16 |
clinically relevant | 16 |
surgical intervention | 16 |
invasive ventilation | 16 |
first patient | 16 |
subjects will | 15 |
primary care | 15 |
ketamine will | 15 |
continuous variables | 15 |
recruitment rate | 15 |
proportional hazards | 15 |
data collected | 15 |
active group | 15 |
irb iec | 15 |
red blood | 15 |
laboratory tests | 15 |
severe respiratory | 15 |
vestibular dysfunction | 15 |
saes will | 15 |
criteria will | 15 |
epithelial cells | 15 |
safety profile | 15 |
local regulations | 15 |
blood cells | 15 |
adverse effects | 15 |
ctcae ratings | 15 |
confirmed covid | 15 |
peep levels | 15 |
cause mortality | 15 |
miracle trial | 15 |
medical record | 15 |
categorical variables | 15 |
will follow | 15 |
critical illness | 15 |
time points | 15 |
risk factor | 15 |
regulatory authorities | 15 |
severe trauma | 15 |
process evaluation | 15 |
protocol items | 15 |
continuous positive | 15 |
cox proportional | 15 |
standard treatment | 15 |
blood cell | 15 |
open label | 15 |
protocol deviations | 15 |
le traitement | 15 |
least years | 15 |
concomitant medication | 15 |
controlled ventilation | 15 |
exact test | 15 |
evaluation period | 15 |
made available | 15 |
digital intervention | 15 |
kg day | 14 |
total sample | 14 |
data safety | 14 |
current study | 14 |
authors read | 14 |
failure assessment | 14 |
sensitivity analyses | 14 |
dementia care | 14 |
pilot study | 14 |
caloric test | 14 |
test will | 14 |
plus soc | 14 |
data entry | 14 |
serum samples | 14 |
days will | 14 |
body weight | 14 |
statistical analyses | 14 |
health care | 14 |
xa activity | 14 |
team will | 14 |
systemic glucocorticoids | 14 |
dose ketamine | 14 |
inhaled sargramostim | 14 |
physician will | 14 |
des patients | 14 |
il inhibitors | 14 |
ethical approval | 14 |
specialist cancer | 14 |
pilot trial | 14 |
primary objective | 14 |
standard care | 14 |
hospital visit | 14 |
aedes aegypti | 14 |
model will | 14 |
final version | 14 |
per protocol | 14 |
trial protocol | 14 |
associated pneumonia | 14 |
path trial | 14 |
secondary outcome | 14 |
subgroup analyses | 14 |
cette recherche | 14 |
induced lung | 14 |
sequential organ | 14 |
month follow | 14 |
inflammatory cytokines | 14 |
ml min | 14 |
will assess | 13 |
resource utilization | 13 |
muscle wasting | 13 |
patients ayant | 13 |
reasonable request | 13 |
sargramostim mcg | 13 |
platelet count | 13 |
treatment allocation | 13 |
clinical effectiveness | 13 |
study personnel | 13 |
regulatory requirements | 13 |
site will | 13 |
secondary objectives | 13 |
ambulatory patients | 13 |
care model | 13 |
health posts | 13 |
acute stroke | 13 |
per arm | 13 |
septal surgery | 13 |
kg min | 13 |
trial steering | 13 |
ct scan | 13 |
pour les | 13 |
eudract number | 13 |
intervention arm | 13 |
partial pressure | 13 |
interventional trials | 13 |
allocation ratio | 13 |
study investigators | 13 |
bloodstream infection | 13 |
increased risk | 13 |
antibiotic treatment | 13 |
early intervention | 13 |
body temperature | 13 |
institutional review | 13 |
quality assurance | 13 |
research council | 13 |
treatment duration | 13 |
acute exacerbation | 13 |
hospital stay | 13 |
iv sargramostim | 13 |
infectious diseases | 13 |
per day | 13 |
rescue intervention | 13 |
protection regulation | 13 |
will evaluate | 13 |
zika virus | 13 |
time frame | 13 |
following criteria | 13 |
inflammatory response | 13 |
cluster randomized | 13 |
indigenous children | 13 |
laboratory parameters | 13 |
i error | 13 |
multicomponent intervention | 12 |
berlin definition | 12 |
ethics approval | 12 |
en cas | 12 |
may require | 12 |
outcomes include | 12 |
peking university | 12 |
tests will | 12 |
long term | 12 |
common terminology | 12 |
future use | 12 |
phase iii | 12 |
pulmonary embolism | 12 |
health research | 12 |
day period | 12 |
comes first | 12 |
oxygen supplementation | 12 |
cancer patients | 12 |
outcome data | 12 |
iu kg | 12 |
virus infection | 12 |
health coaching | 12 |
allergic reactions | 12 |
cluster randomised | 12 |
survivorship care | 12 |
peripheral blood | 12 |
mcg ml | 12 |
first hospital | 12 |
compared using | 12 |
controlled study | 12 |
visits will | 12 |
calendar days | 12 |
inflammatory markers | 12 |
ravulizumab will | 12 |
white blood | 12 |
protocol adherence | 12 |
surface area | 12 |
treatment effect | 12 |
review board | 12 |
en charge | 12 |
confirmed cases | 12 |
direct access | 12 |
approximately patients | 12 |
inferiority margin | 12 |
will allow | 12 |
clinical outcome | 12 |
data capture | 12 |
whichever comes | 12 |
control groups | 12 |
adverse reactions | 12 |
will meet | 12 |
respiratory disease | 12 |
participant will | 12 |
study staff | 12 |
intervention strategy | 12 |
university first | 12 |
nursing home | 12 |
rm max | 12 |
body surface | 12 |
pulse oximetry | 12 |
prep group | 12 |
dans un | 12 |
will ensure | 12 |
standard practice | 12 |
consent forms | 12 |
candidate agents | 12 |
dietary quality | 12 |
systemic inflammation | 12 |
patients infected | 11 |
sargramostim affects | 11 |
take part | 11 |
edta blood | 11 |
chez les | 11 |
will conduct | 11 |
body mass | 11 |
pendant jours | 11 |
temporal relationship | 11 |
patients undergoing | 11 |
trial participants | 11 |
general data | 11 |
randomisation will | 11 |
years old | 11 |
procedure will | 11 |
calculated using | 11 |
patients treated | 11 |
cardiovascular disease | 11 |
respiratory support | 11 |
bacterial pathogens | 11 |
descriptive statistics | 11 |
versus days | 11 |
study visit | 11 |
terminology criteria | 11 |
adjunct low | 11 |
treatment period | 11 |
square test | 11 |
medication will | 11 |
will perform | 11 |
birth weight | 11 |
gas analysis | 11 |
ml kg | 11 |
ovid study | 11 |
active surveillance | 11 |
deemed necessary | 11 |
weeks prior | 11 |
replacement therapy | 11 |
healthcare providers | 11 |
research project | 11 |
respiratory system | 11 |
groups using | 11 |
binary outcome | 11 |
within weeks | 11 |
will make | 11 |
health system | 11 |
fibrosis bronchiectasis | 11 |
chronic lung | 11 |
pro data | 11 |
study groups | 11 |
male patients | 11 |
retrograde cholangiopancreatography | 11 |
trial registry | 11 |
baseline data | 11 |
ventilatory support | 11 |
endoscopic retrograde | 11 |
infants hospitalised | 11 |
patients included | 11 |
treating physicians | 11 |
recovery time | 11 |
among patients | 11 |
past months | 11 |
last patient | 11 |
health districts | 11 |
study results | 11 |
chronic respiratory | 11 |
day onwards | 11 |
outcome measure | 11 |
additional days | 11 |
abv illness | 11 |
flow oxygen | 11 |
final follow | 11 |
whole blood | 11 |
respiratory infection | 11 |
lower respiratory | 11 |
prise en | 11 |
clinical recovery | 11 |
medical sciences | 11 |
endpoint will | 11 |
flow rate | 11 |
ethical committee | 11 |
patients experiencing | 11 |
national institute | 11 |
may th | 11 |
coaching sessions | 11 |
hospital records | 11 |
feasibility study | 10 |
investigational product | 10 |
positive pressure | 10 |
ambulatory treatment | 10 |
observational study | 10 |
last infusion | 10 |
master protocol | 10 |
allocation will | 10 |
parameters will | 10 |
childbearing potential | 10 |
group sequential | 10 |
will consist | 10 |
ae sae | 10 |
high flow | 10 |
will submit | 10 |
first patients | 10 |
total number | 10 |
nasal cannula | 10 |
time point | 10 |
attending physician | 10 |
viral infections | 10 |
will undergo | 10 |
mg per | 10 |
des personnes | 10 |
stimulating factor | 10 |
syndrome coronavirus | 10 |
clinical characteristics | 10 |
mass index | 10 |
kg twice | 10 |
secondary analyses | 10 |
viral infection | 10 |
month period | 10 |
northern territory | 10 |
treat analysis | 10 |
safety outcomes | 10 |
statistical code | 10 |
participant recruitment | 10 |
will review | 10 |
study sites | 10 |
final analysis | 10 |
complement system | 10 |
best supportive | 10 |
study outcomes | 10 |
ward patients | 10 |
nasal septum | 10 |
electronic case | 10 |
abv infection | 10 |
study information | 10 |
safety data | 10 |
mg sarilumab | 10 |
data set | 10 |
fondation adolphe | 10 |
competent authority | 10 |
receive standard | 10 |
patient safety | 10 |
treating clinician | 10 |
respiratory viruses | 10 |
patient data | 10 |
filled syringes | 10 |
mitochondrial dna | 10 |
protocol will | 10 |
arterial pressure | 10 |
applicable regulatory | 10 |
two study | 10 |
american society | 10 |
higher peep | 10 |
influenza virus | 10 |
atrial fibrillation | 10 |
nasal oxygen | 10 |
unexpected serious | 10 |
sae reporting | 10 |
taking part | 10 |
baseline characteristics | 10 |
ischemic stroke | 10 |
drug will | 10 |
au cours | 10 |
renal replacement | 10 |
measurements will | 10 |
will improve | 10 |
regression model | 10 |
patients randomised | 10 |
dose lmwh | 10 |
will compare | 10 |
sample will | 10 |
interquartile range | 10 |
chloride injection | 10 |
recruit patients | 10 |
sponsor will | 10 |
schools will | 10 |
day treatment | 10 |
symptomatic abv | 10 |
computed tomography | 10 |
hypertension treatment | 10 |
regression models | 10 |
reported outcomes | 10 |
current treatment | 10 |
reactive protein | 10 |
allocation sequence | 10 |
renal failure | 10 |
ciprofloxacin mg | 10 |
becoming aware | 10 |
randomization stratification | 10 |
abv transmission | 10 |
health behaviours | 10 |
may include | 10 |
stratification factor | 10 |
statistically significant | 10 |
medical research | 10 |
risk assessment | 10 |
will recruit | 10 |
implementation strategies | 9 |
barthel index | 9 |
category ordinal | 9 |
ctcae rating | 9 |
deep sedation | 9 |
family members | 9 |
sufficient time | 9 |
treatment arm | 9 |
accompanying person | 9 |
will remain | 9 |
two arms | 9 |
cause death | 9 |
conventional therapy | 9 |
le groupe | 9 |
respiratory syncytial | 9 |
zealand clinical | 9 |
hpa axis | 9 |
may lead | 9 |
nurses will | 9 |
period will | 9 |
protocol analysis | 9 |
care units | 9 |
bleeding requiring | 9 |
regression will | 9 |
retrospective cohort | 9 |
bronchiectasis exacerbations | 9 |
day compared | 9 |
please see | 9 |
randomised trials | 9 |
investigator may | 9 |
treat principle | 9 |
least weeks | 9 |
reference number | 9 |
commonly used | 9 |
polymerase chain | 9 |
controlled clinical | 9 |
laboratory test | 9 |
kidney function | 9 |
covid patients | 9 |
sartre study | 9 |
first dose | 9 |
trial data | 9 |
mean change | 9 |
national cancer | 9 |
study population | 9 |
clinical course | 9 |
every hours | 9 |
multiple imputation | 9 |
immune response | 9 |
fio ratio | 9 |
every day | 9 |
widely used | 9 |
patients without | 9 |
uz ghent | 9 |
treatment assignment | 9 |
phone call | 9 |
antibiotic therapy | 9 |
blood serum | 9 |
day visit | 9 |
medical care | 9 |
blood tests | 9 |
will report | 9 |
endpoints will | 9 |
continuous infusion | 9 |
medical treatment | 9 |
single iv | 9 |
study eudract | 9 |
health status | 9 |
liver function | 9 |
must also | 9 |
safety information | 9 |
investigational site | 9 |
respiratory exacerbations | 9 |
patients requiring | 9 |
rater reliability | 9 |
respiratory elastance | 9 |
patient recruited | 9 |
bsc will | 9 |
molecular patterns | 9 |
children will | 9 |
molecular weight | 9 |
relevant bleeding | 9 |
days number | 9 |
visit will | 9 |
population will | 9 |
protocol deviation | 9 |
turbinate reduction | 9 |
documents will | 9 |
individual patient | 9 |
reported outcome | 9 |
will reduce | 9 |
chronic cough | 9 |
antiplatelet therapy | 9 |
provide informed | 9 |
delivery room | 9 |
legal representative | 9 |
energy homeostasis | 9 |
highly effective | 9 |
administered intravenously | 9 |
confidence intervals | 9 |
peripheral vestibular | 9 |
report will | 9 |
will collect | 9 |
elderly patients | 9 |
glasgow coma | 9 |
induced thrombocytopenia | 9 |
national institutes | 9 |
immune system | 9 |
clinical decision | 9 |
un traitement | 9 |
hospitalised patients | 9 |
random numbers | 9 |
monitoring plan | 9 |
form will | 9 |
united states | 9 |
thromboembolic complications | 9 |
spo fio | 9 |
vasoplegic shock | 9 |
mg day | 9 |
alexion confidential | 9 |
arterial oxygen | 9 |
severe air | 9 |
pressure ventilation | 9 |
severe ards | 9 |
chain reaction | 9 |
icu units | 9 |
forms will | 9 |
final report | 9 |
gov nct | 9 |
committee will | 9 |
will require | 9 |
based system | 9 |
least days | 9 |
respiratory bacterial | 9 |
age group | 9 |
emory university | 9 |
associated molecular | 9 |
treatment success | 9 |
biological specimens | 9 |
baseline severity | 9 |
one patient | 9 |
main rct | 9 |
analogue scale | 9 |
mechanical ventilatory | 9 |
therapeutic response | 9 |
congenital anomaly | 8 |
treat population | 8 |
peak inspiratory | 8 |
investigational medicinal | 8 |
potential participants | 8 |
drug administration | 8 |
pas totalement | 8 |
health centers | 8 |
weeks post | 8 |
experimental therapy | 8 |
clinical management | 8 |
months prior | 8 |
hazards model | 8 |
original treatment | 8 |
les informations | 8 |
patient recruitment | 8 |
systolic blood | 8 |
data sharing | 8 |
health outcomes | 8 |
daily doses | 8 |
aes will | 8 |
important protocol | 8 |
endotracheal tube | 8 |
sur le | 8 |
intervention groups | 8 |
anticoagulant treatment | 8 |
versus usual | 8 |
current standard | 8 |
additional blood | 8 |
surfactant administration | 8 |
au promoteur | 8 |
envelopes will | 8 |
reasonable possibility | 8 |
saudi arabia | 8 |
general hospital | 8 |
hazard ratio | 8 |
aged years | 8 |
neutrophil extracellular | 8 |
interstitial pneumonia | 8 |
reported within | 8 |
clinical follow | 8 |
every months | 8 |
implementation process | 8 |
qui se | 8 |
concomitant drug | 8 |
screen failure | 8 |
reviewed journals | 8 |
vein thrombosis | 8 |
trial results | 8 |
last days | 8 |
enoxaparin will | 8 |
research center | 8 |
jwby formulas | 8 |
inflammatory processes | 8 |
combination therapy | 8 |
four groups | 8 |
take oral | 8 |
fatality rate | 8 |
treatment guidelines | 8 |
baseline visit | 8 |
requiring invasive | 8 |
severe renal | 8 |
last visit | 8 |
intravenous infusion | 8 |
group assignment | 8 |
research nurse | 8 |
within months | 8 |
study group | 8 |
low birth | 8 |
previous studies | 8 |
weight heparin | 8 |
huashan hospital | 8 |
secondary analysis | 8 |
ris group | 8 |
protocol violations | 8 |
face mask | 8 |
balance rct | 8 |
outcome assessment | 8 |
epidemiological impact | 8 |
respiratory pathogens | 8 |
functional assessment | 8 |
asthma patients | 8 |
acutely ill | 8 |
study participant | 8 |
treatment effects | 8 |
wilcoxon rank | 8 |
end point | 8 |
room air | 8 |
oxygen supplement | 8 |
version number | 8 |
ten days | 8 |
thromboembolic events | 8 |
die within | 8 |
middle east | 8 |
drugs will | 8 |
values will | 8 |
international guidelines | 8 |
study records | 8 |
routine clinical | 8 |
additional information | 8 |
mean difference | 8 |
first year | 8 |
care services | 8 |
innate immune | 8 |
mashhad university | 8 |
third party | 8 |
creatinine clearance | 8 |
normally distributed | 8 |
nasal airway | 8 |
centers will | 8 |
east respiratory | 8 |
score odoratest | 8 |
proactive prophylaxis | 8 |
alternative explanation | 8 |
next exacerbation | 8 |
patients covid | 8 |
pk pd | 8 |
eminent intervention | 8 |
ayant une | 8 |
chloroquine phosphate | 8 |
patients receiving | 8 |
syncytial virus | 8 |
placebo group | 8 |
axillary temperature | 8 |
blood count | 8 |
lung recruitment | 8 |
general anaesthesia | 8 |
avant le | 8 |
day prednisone | 8 |
des lavages | 8 |
international conference | 8 |
may affect | 8 |
peep level | 8 |
fudan university | 8 |
sc injection | 8 |
national health | 8 |
patients suffering | 8 |
local ethics | 8 |
event one | 8 |
test results | 8 |
yucatan state | 8 |
spontaneous breathing | 8 |
iv injection | 8 |
assessment scales | 8 |
block sizes | 8 |
ventilation mode | 8 |
medical condition | 8 |
dsmb will | 8 |
mg ravulizumab | 8 |
nasal patency | 8 |
trial statistician | 8 |
concomitant disease | 8 |
severe adverse | 8 |
inflammatory effect | 8 |
dmc will | 8 |
rheumatoid arthritis | 8 |
alveolar macrophages | 8 |
related quality | 8 |
days alive | 8 |
randomized control | 8 |
data entries | 8 |
cancer nurse | 8 |
information provided | 8 |
room temperature | 7 |
contact person | 7 |
traditional chinese | 7 |
center will | 7 |
confirmed probable | 7 |
sarilumab will | 7 |
visual analogue | 7 |
prior balance | 7 |
pulmonary hypertension | 7 |
study procedure | 7 |
asthma assessment | 7 |
gcp guidelines | 7 |
health services | 7 |
recruitment rates | 7 |
glucocorticoid therapy | 7 |
exacerbations per | 7 |
therefore believe | 7 |
interviews will | 7 |
recruitment will | 7 |
eortc qlq | 7 |
specimens will | 7 |
systemic inflammatory | 7 |
label trial | 7 |
positive sars | 7 |
australian indigenous | 7 |
uncorrected axillary | 7 |
significantly reduced | 7 |
repeated sc | 7 |
data must | 7 |
practice guidelines | 7 |
storage conditions | 7 |
care coordination | 7 |
large number | 7 |
group allocation | 7 |
aerosolized dornase | 7 |
clinically appropriate | 7 |
peep range | 7 |
educational module | 7 |
financial toxicity | 7 |
laboratory results | 7 |
placebo arm | 7 |
china clinical | 7 |
sum test | 7 |
kg body | 7 |
prevent one | 7 |
author details | 7 |
abv cases | 7 |
ae crf | 7 |
versus medical | 7 |
missing values | 7 |
improve survival | 7 |
standard hygiene | 7 |
random number | 7 |
viral load | 7 |
community health | 7 |
nitrogen balance | 7 |
acacia senegal | 7 |
study subjects | 7 |
allocated treatment | 7 |
les investigateurs | 7 |
nasopharyngeal swab | 7 |
methods design | 7 |
vital parameters | 7 |
ordinating investigator | 7 |
selon les | 7 |
extracellular traps | 7 |
registration number | 7 |
primary endpoints | 7 |
clinical worsening | 7 |
known hypersensitivity | 7 |
will help | 7 |
ill medical | 7 |
future research | 7 |
complex interventions | 7 |
assess whether | 7 |
treatment protocol | 7 |
tract infection | 7 |
chlamydia species | 7 |
rank sum | 7 |
study aims | 7 |
two different | 7 |
ng ml | 7 |
icu wards | 7 |
alanine aminotransferase | 7 |
collect peripheral | 7 |
study conduct | 7 |
versus standard | 7 |
elevated il | 7 |
control program | 7 |
medical monitor | 7 |
ctu will | 7 |
ventilation strategy | 7 |
process will | 7 |
block randomization | 7 |
implementation research | 7 |
feasibility outcomes | 7 |
high levels | 7 |
mg orally | 7 |
lung diseases | 7 |
coronavirus infection | 7 |
disease requiring | 7 |
inflammatory parameters | 7 |
hyperinflammatory syndrome | 7 |
serum ferritin | 7 |
intravenous injection | 7 |
patients recruited | 7 |
le cadre | 7 |
ghent university | 7 |
high dose | 7 |
symptomatic vte | 7 |
blood test | 7 |
th day | 7 |
receive placebo | 7 |
animal models | 7 |
conditional recommendation | 7 |
deviated septum | 7 |
ethics committees | 7 |
days prior | 7 |
meningococcal vaccination | 7 |
clinical benefit | 7 |
intervention clinician | 7 |
study duration | 7 |
research nurses | 7 |
liver disease | 7 |
receive either | 7 |
reference group | 7 |
may reduce | 7 |
children aged | 7 |
severe pollution | 7 |
prone positioning | 7 |
multiorgan failure | 7 |
secondary efficacy | 7 |
following variables | 7 |
factors associated | 7 |
per local | 7 |
include patients | 7 |
single mg | 7 |
ravulizumab treatment | 7 |
le protocole | 7 |
oral consent | 7 |
du protocole | 7 |
whenever possible | 7 |
will obtain | 7 |
jun page | 7 |
will determine | 7 |
brain injury | 7 |
records may | 7 |
du traitement | 7 |
gestational age | 7 |
study database | 7 |
partner therapeutics | 7 |
task force | 7 |
per standard | 7 |
evaluation will | 7 |
randomly allocated | 7 |
oral anticoagulants | 7 |
secondary aim | 7 |
funding body | 7 |
recent laboratory | 7 |
reduced mobility | 7 |
caregiver burden | 7 |
nursing homes | 7 |
will participate | 7 |
give consent | 7 |
recommended dose | 7 |
enteral nutrition | 7 |
control trial | 7 |
three times | 7 |
failure requiring | 7 |
income countries | 7 |
data integrity | 7 |
competent authorities | 7 |
will serve | 7 |
infectious disease | 7 |
requiring dialysis | 7 |
oxygenation parameters | 7 |
per month | 7 |
cancer institute | 7 |
will maintain | 7 |
concomitant medications | 7 |
disease management | 7 |
colony stimulating | 7 |
lung repair | 7 |
gov identifier | 7 |
bloodstream infections | 7 |
viral respiratory | 7 |
csf treatment | 7 |
health evaluation | 7 |
alternative hypothesis | 7 |
least months | 7 |
european union | 7 |
les deux | 7 |
allocation concealment | 7 |
care pathway | 7 |
related monitoring | 7 |
invasive procedures | 7 |
local clinical | 7 |
representative will | 7 |
idiopathic sudden | 7 |
participating sites | 7 |
serum blood | 7 |
trial dataset | 7 |
independent data | 7 |
chinese medicine | 7 |
des signes | 7 |
effects will | 7 |
nitric oxide | 7 |
behavior change | 7 |
pulmonary function | 7 |
passive surveillance | 7 |
positive test | 7 |
early breast | 7 |
le patient | 7 |
will generate | 7 |
mean arterial | 7 |
indigenous australian | 7 |
randomized placebo | 6 |
disseminated intravascular | 6 |
intermittent positive | 6 |
site file | 6 |
product information | 6 |
total duration | 6 |
negative pregnancy | 6 |
icu versus | 6 |
en lavage | 6 |
elastance peep | 6 |
ventilator dyssynchrony | 6 |
monitor will | 6 |
live intervention | 6 |
discharge whichever | 6 |
study id | 6 |
therapy will | 6 |
implementation outcomes | 6 |
procedures will | 6 |
tidal volumes | 6 |
oxygen delivery | 6 |
blood will | 6 |
rct will | 6 |
mrs score | 6 |
day follow | 6 |
pulmonary hemorrhage | 6 |
mcg twice | 6 |
pollution monitoring | 6 |
will inform | 6 |
stored samples | 6 |
potential risk | 6 |
ml solution | 6 |
occult blood | 6 |
telephone calls | 6 |
vast majority | 6 |
bsc compared | 6 |
venous blood | 6 |
sc administration | 6 |
sequence will | 6 |
written information | 6 |
sedative agent | 6 |
will coordinate | 6 |
nasal continuous | 6 |
well tolerated | 6 |
hospitalized across | 6 |
lung damage | 6 |
volunteer support | 6 |
minimum elastance | 6 |
antibiotic arm | 6 |
cov test | 6 |
sites will | 6 |
statistical significance | 6 |
test result | 6 |
based dose | 6 |
foreseeable overflow | 6 |
care patients | 6 |
odds ratio | 6 |
healthcare system | 6 |
selected centers | 6 |
see section | 6 |
tract infections | 6 |
clinical assessment | 6 |
study nurse | 6 |
study day | 6 |
data documents | 6 |
intravascular coagulation | 6 |
will record | 6 |
points au | 6 |
progressive patients | 6 |
regulatory agency | 6 |
month intervention | 6 |
jours du | 6 |
local principal | 6 |
safety reasons | 6 |
following parameters | 6 |
determine whether | 6 |
proinflammatory cytokines | 6 |
balance pilot | 6 |
hygiene requirements | 6 |
care setting | 6 |
peep selection | 6 |
cancer centre | 6 |
component summary | 6 |
median time | 6 |
stage design | 6 |
vestibular pathway | 6 |
severe sepsis | 6 |
medical illnesses | 6 |
evoked myogenic | 6 |
block size | 6 |
patients progressing | 6 |
normal range | 6 |
oral prednisone | 6 |
pain score | 6 |
viral disease | 6 |
care medicine | 6 |
serum pregnancy | 6 |
randomised trial | 6 |
statistics will | 6 |
semicircular canal | 6 |
emergency department | 6 |
urea nitrogen | 6 |
design will | 6 |
thoracic society | 6 |
study entry | 6 |
adult respiratory | 6 |
muscle protein | 6 |
health district | 6 |
disc annulus | 6 |
case reports | 6 |
laboratory testing | 6 |
clinical examination | 6 |
tidal volume | 6 |
nasal septal | 6 |
size will | 6 |
days time | 6 |
short term | 6 |
suspected unexpected | 6 |
ventilator settings | 6 |
residual insecticides | 6 |
maximal value | 6 |
maximal increase | 6 |
lung inflammation | 6 |
en france | 6 |
will need | 6 |
subjects may | 6 |
models will | 6 |
final concentration | 6 |
kg every | 6 |
experimental arm | 6 |
detailed statistical | 6 |
au score | 6 |
method will | 6 |
performed according | 6 |
peep cmh | 6 |
maximum dose | 6 |
hyposmie persistante | 6 |
identifying information | 6 |
done using | 6 |
main secondary | 6 |
receive prophylactic | 6 |
pg ml | 6 |
severely ill | 6 |
flow cytometric | 6 |
hypertensive patients | 6 |
retrospective study | 6 |
doses will | 6 |
unless otherwise | 6 |
dose time | 6 |
factorial design | 6 |
based approach | 6 |
fasting blood | 6 |
trial team | 6 |
collect data | 6 |
event rate | 6 |
cpap failure | 6 |
outpatient visits | 6 |
study centre | 6 |
symptom onset | 6 |
may receive | 6 |
primary end | 6 |
oxygen requirement | 6 |
linear regression | 6 |
binary logistic | 6 |
qualitative interviews | 6 |
study sponsor | 6 |
alternative treatment | 6 |
avec les | 6 |
study interventions | 6 |
health professionals | 6 |
specific procedures | 6 |
plague patients | 6 |
assessed using | 6 |
coordinator will | 6 |
underlying disease | 6 |
vanderbilt university | 6 |
trial sponsor | 6 |
urgent need | 6 |
peripheral capillary | 6 |
spike protein | 6 |
outcome test | 6 |
disease severity | 6 |
number will | 6 |
life expectancy | 6 |
ethical committees | 6 |
study arms | 6 |
total patients | 6 |
develop respiratory | 6 |
clarify whether | 6 |
au long | 6 |
cumulative incidence | 6 |
called group | 6 |
considered serious | 6 |
mild general | 6 |
health behaviour | 6 |
cell count | 6 |
database will | 6 |
chronic kidney | 6 |
system elastance | 6 |
probable covid | 6 |
trial conduct | 6 |
iu ml | 6 |
vital status | 6 |
statistical power | 6 |
give access | 6 |
confirmed symptomatic | 6 |
entre les | 6 |
will still | 6 |
following events | 6 |
group compared | 6 |
standard supportive | 6 |
viral pneumonia | 6 |
demographic data | 6 |
pi will | 6 |
corona virus | 6 |
sectional study | 6 |
management group | 6 |
label study | 6 |
copd exacerbations | 6 |
assessments will | 6 |
enrolled participants | 6 |
stopping rules | 6 |
bubo size | 6 |
within one | 6 |
safety assessments | 6 |
medical intervention | 6 |
trial comparing | 6 |
days within | 6 |
global burden | 6 |
following treatment | 6 |
conducted according | 6 |
dengue virus | 6 |
treatment plan | 6 |
day intervention | 6 |
abv case | 6 |
terminal complement | 6 |
point ordinal | 6 |
clinical evidence | 6 |
diastolic blood | 6 |
adult inpatients | 6 |
report forms | 6 |
cov testing | 6 |
severe cases | 6 |
current use | 6 |
nervous system | 6 |
traitement local | 6 |
le cahier | 6 |
huge impact | 6 |
telephone call | 6 |
monitoring will | 6 |
study number | 6 |
daily clinical | 6 |
trial participation | 6 |
potential risks | 6 |
cancer nurses | 6 |
iv twice | 6 |
evaluate differences | 6 |
kidney disease | 6 |
bacterial infections | 6 |
intravenously following | 6 |
early acute | 6 |
clinical judgement | 6 |
personal information | 6 |
meier plot | 6 |
targeted indoor | 6 |
blood markers | 6 |
trial medications | 6 |
alexion gds | 6 |
monoclonal antibody | 6 |
oral administration | 6 |
trial master | 6 |
cov infection | 6 |
coma scale | 6 |
une hyposmie | 6 |
every participant | 6 |
wedge randomized | 6 |
proven effective | 6 |
inhaled iloprost | 6 |
usual activities | 6 |
pain scale | 6 |
evidence base | 6 |
results may | 6 |
pilot randomized | 6 |
potential benefits | 6 |
mean airway | 6 |
emergency visits | 6 |
four weeks | 6 |
pregnant women | 6 |
early nasal | 6 |
intervention program | 6 |
management plan | 6 |
capillary oxygen | 6 |
nucleic acid | 6 |
final study | 6 |
outcome analysis | 6 |
mise en | 6 |
patients must | 6 |
study coordinator | 6 |
personne qui | 6 |
doctor will | 6 |
sae form | 6 |
outpatient setting | 6 |
spirit checklist | 6 |
coagulation activation | 6 |
physical examinations | 6 |
spending function | 6 |
human use | 6 |
alexion will | 6 |
safety reporting | 6 |
australian infants | 6 |
verbal consent | 6 |
otitis media | 6 |
data sets | 6 |
participant information | 6 |
cardiovascular events | 6 |
database lock | 6 |
product characteristics | 6 |
cancer specialists | 6 |
without prior | 6 |
records will | 6 |
edta tube | 6 |
master file | 6 |
general covid | 6 |
control ventilation | 6 |
macrophage colony | 6 |
study related | 6 |
acute exacerbations | 6 |
nairos trial | 6 |
tcm syndrome | 6 |
sarilumab plus | 6 |
du produit | 6 |
multicomponent program | 6 |
medical ethics | 6 |
hearing outcomes | 6 |
bushen yiqi | 6 |
systematic analysis | 6 |
related documents | 6 |
synbiotic supplementation | 6 |
study centers | 6 |
mental health | 6 |
entire study | 6 |
acute vte | 6 |
protective ventilation | 6 |
researchers will | 6 |
hospital clinic | 6 |
motivational interviewing | 5 |
currently ongoing | 5 |
systemic glucocorticoid | 5 |
streptococcus pneumoniae | 5 |
aviez avant | 5 |
data confidentiality | 5 |
details key | 5 |
acute ischemic | 5 |
secondary endpoint | 5 |
closely monitored | 5 |
failure nyha | 5 |
laboratory abnormality | 5 |
noninvasive ventilation | 5 |
medenox study | 5 |
will contact | 5 |
sensitivity analysis | 5 |
personne humaine | 5 |
laboratory abnormalities | 5 |
project will | 5 |
null hypothesis | 5 |
provide written | 5 |
many years | 5 |
contact details | 5 |
patient withdraws | 5 |
staircase recruitment | 5 |
form must | 5 |
participants per | 5 |
cancer therapy | 5 |
blood sampling | 5 |
recruitment intervention | 5 |
rising since | 5 |
randomization sequence | 5 |
antiviral immunity | 5 |
safety population | 5 |
ae will | 5 |
chinese version | 5 |
collection will | 5 |
efficacy endpoint | 5 |
interstitial lung | 5 |
using sas | 5 |
list will | 5 |
nasal blockage | 5 |
cancer treatment | 5 |
normal saline | 5 |
samples collected | 5 |
randomized patients | 5 |
care treatment | 5 |
pulmonary alveolar | 5 |
laboratory evaluation | 5 |
health benefits | 5 |
coordinating center | 5 |
diabetes mellitus | 5 |
older patients | 5 |
hormonal contraception | 5 |
considered clinically | 5 |
based method | 5 |
confirmed sars | 5 |
ii trial | 5 |
investigational therapy | 5 |
septal deviation | 5 |
infants will | 5 |
prophylactic antibiotics | 5 |
study effects | 5 |
will contain | 5 |
designee will | 5 |
recruitment started | 5 |
amendments will | 5 |
protection act | 5 |
nursing staff | 5 |
benefit assessment | 5 |
preventing progression | 5 |
streptomycin plus | 5 |
high incidence | 5 |
inner ear | 5 |
signs symptoms | 5 |
treatment strategies | 5 |
bleeding events | 5 |
alexion within | 5 |
renal insufficiency | 5 |
respiratory medicine | 5 |
pour chaque | 5 |
relief therapy | 5 |
cognitive impairment | 5 |
patient per | 5 |
per minute | 5 |
additional doses | 5 |
two large | 5 |
university will | 5 |
legal guardian | 5 |
risks associated | 5 |
investigate whether | 5 |
enrolled patients | 5 |
outcome assessors | 5 |
hour intravenous | 5 |
authorized site | 5 |
treatments will | 5 |
hypertensive care | 5 |
mechanical ventilator | 5 |
past days | 5 |
du code | 5 |
intravenous sargramostim | 5 |
study specific | 5 |
bilateral infiltrates | 5 |
poisson regression | 5 |
administer enoxaparin | 5 |
treatment follow | 5 |
level data | 5 |
clinical diagnosis | 5 |
since last | 5 |
deemed clinically | 5 |
heart disease | 5 |
dosing days | 5 |
respiratory function | 5 |
performance status | 5 |
serum levels | 5 |
sedation protocol | 5 |
laboratory reports | 5 |
subgroup analysis | 5 |
will lead | 5 |
baseline will | 5 |
tcm herbs | 5 |
patient experience | 5 |
improve outcome | 5 |
trials group | 5 |
become available | 5 |
present study | 5 |
permit study | 5 |
trial future | 5 |
general medical | 5 |
project management | 5 |
package insert | 5 |
chronic rhinosinusitis | 5 |
current ascending | 5 |
deux bras | 5 |
patients site | 5 |
considered significant | 5 |
une seule | 5 |
best interests | 5 |
significantly reduce | 5 |
data analysts | 5 |
relevant parties | 5 |
overall sample | 5 |
year follow | 5 |
strictly confidential | 5 |
patients rising | 5 |
linear mixed | 5 |
extracorporeal membrane | 5 |
procedural sedation | 5 |
gentofte hospital | 5 |
nasal intermittent | 5 |
secondary haemophagocytic | 5 |
will describe | 5 |
must use | 5 |
receive mg | 5 |
sarilumab dose | 5 |
continue antibiotic | 5 |
asthma exacerbation | 5 |
time required | 5 |
support behaviour | 5 |
bleeding diathesis | 5 |
minute ventilation | 5 |
requiring mechanical | 5 |
early treatment | 5 |
target sample | 5 |
blood specimens | 5 |
turkish study | 5 |
may prevent | 5 |
vestibular evoked | 5 |
permuted blocks | 5 |
laboratory data | 5 |
previous page | 5 |
hypertensive medications | 5 |
iu anti | 5 |
study designed | 5 |
cancer survivorship | 5 |
efficacy endpoints | 5 |
term systemic | 5 |
european consensus | 5 |
amino acid | 5 |
clinical team | 5 |
updated guidelines | 5 |
negative bacteria | 5 |
fatty acids | 5 |
patient enrolment | 5 |
different peep | 5 |
randomized using | 5 |
trial arms | 5 |
fatal consequences | 5 |
intervention may | 5 |
data manager | 5 |
enrolled children | 5 |
child health | 5 |
signed consent | 5 |
weight infants | 5 |
endotracheal intubation | 5 |
par pcr | 5 |
recruitment manoeuvres | 5 |
suspected cases | 5 |
global health | 5 |
inhaled gm | 5 |
lung homeostasis | 5 |
max mg | 5 |
nose score | 5 |
control schools | 5 |
withdrawal will | 5 |
blood transfusion | 5 |
following conditions | 5 |
acetylsalicylic acid | 5 |
ventilation will | 5 |
dose pre | 5 |
airway obstruction | 5 |
female partner | 5 |
pulp stem | 5 |
consent process | 5 |
statistical software | 5 |
susceptibility testing | 5 |
iv infusion | 5 |
proposed protocol | 5 |
either oral | 5 |
estimated using | 5 |
final data | 5 |
codes will | 5 |
management arm | 5 |
baseline values | 5 |
mean number | 5 |
intervention schools | 5 |
stable chronic | 5 |
discharge letters | 5 |
collected data | 5 |
deep vein | 5 |
central vestibular | 5 |
stratified analyzes | 5 |
privacy protection | 5 |
treatments directed | 5 |
viral replication | 5 |
positive serology | 5 |
days free | 5 |
research staff | 5 |
le cas | 5 |
une atteinte | 5 |
upright position | 5 |
dose mg | 5 |
trial management | 5 |
sae reports | 5 |
function test | 5 |
transmission season | 5 |
support within | 5 |
authors contributed | 5 |
insecticide resistance | 5 |
screen failures | 5 |
withdraw consent | 5 |
epidemiology curve | 5 |
clinical presentation | 5 |
primary investigator | 5 |
upper limit | 5 |
abv infections | 5 |
original data | 5 |
intracranial hemorrhage | 5 |
cure software | 5 |
care will | 5 |
year increase | 5 |
will enter | 5 |
hearing outcome | 5 |
trial aims | 5 |
required sample | 5 |
rankin scale | 5 |
communicating important | 5 |
study arm | 5 |
sore throat | 5 |
safety outcome | 5 |
two additional | 5 |
important medical | 5 |
events occurring | 5 |
substantial amendments | 5 |
case series | 5 |
increased levels | 5 |
study nurses | 5 |
internal medicine | 5 |
shared care | 5 |
abnormal laboratory | 5 |
ascending part | 5 |
inflammatory cytokine | 5 |
plot will | 5 |
minimal elastance | 5 |
just days | 5 |
lung compliance | 5 |
new therapeutic | 5 |
consolidated standards | 5 |
family member | 5 |
publicly available | 5 |
long cours | 5 |
admitted confirmed | 5 |
central ec | 5 |
breathing room | 5 |
six months | 5 |
possible adverse | 5 |
vous aviez | 5 |
analysts will | 5 |
nyha iii | 5 |
system will | 5 |
study found | 5 |
will ask | 5 |
fulfilling inclusion | 5 |
safety report | 5 |
vestibular system | 5 |
nasal spray | 5 |
adjusted analysis | 5 |
requiring hospitalization | 5 |
elevated levels | 5 |
general practitioners | 5 |
unfractionated heparin | 5 |
medical staff | 5 |
infusion reaction | 5 |
will attempt | 5 |
daily dose | 5 |
acute phase | 5 |
functional outcome | 5 |
female subjects | 5 |
multi organ | 5 |
corticosteroids will | 5 |
acute pulmonary | 5 |
chronic condition | 5 |
interventions will | 5 |
avian influenza | 5 |
acute physiology | 5 |
see table | 5 |
temporary cessation | 5 |
bronchodilator reversibility | 5 |
aspartate aminotransferase | 5 |
two independent | 5 |
mixed models | 5 |
antibiotic resistance | 5 |
treatment failure | 5 |
amoxicillinclavulanic acid | 5 |
australian institute | 5 |
copd gold | 5 |
statistician will | 5 |
modified rankin | 5 |
summary statistics | 5 |
mesh nebulizer | 5 |
final clinical | 5 |
data verification | 5 |
level will | 5 |
covid scale | 5 |
considered eligible | 5 |
reporting parallel | 5 |
like receptors | 5 |
ent hospital | 5 |
sae data | 5 |
activity levels | 5 |
usual hypertensive | 5 |
services will | 5 |
superior vestibular | 5 |
study enrolment | 5 |
muscle relaxants | 5 |
chronic suppurative | 5 |
participants may | 5 |
birth defect | 5 |
unplanned outpatient | 5 |
uz gent | 5 |
alternate aetiology | 5 |
standard oxygen | 5 |
jugement principal | 5 |
following secondary | 5 |
dendritic cells | 5 |
molecular analysis | 5 |
care physicians | 5 |
orally twice | 5 |
treated patients | 5 |
suppurative lung | 5 |
occurring within | 5 |
intellectual content | 5 |
treat patients | 5 |
balance trial | 5 |
consenting process | 5 |
will focus | 5 |
venous thromboembolic | 5 |
label clinical | 5 |
settings will | 5 |
haemophagocytic lymphohistiocytosis | 5 |
study must | 5 |
approximately months | 5 |
ventilated trauma | 5 |
azienda ospedaliero | 5 |
south australia | 5 |
significant portion | 5 |
line personnel | 5 |
coronary syndrome | 5 |
service innovation | 5 |
improve hypertension | 5 |
reporting structure | 5 |
data quality | 5 |
membrane oxygenation | 5 |
medicina interna | 5 |
trial care | 5 |
randomization codes | 5 |
hcs training | 5 |
adverse drug | 5 |
clinical protocol | 5 |
ordinal logistic | 5 |
care alone | 5 |
containing mg | 5 |
will consider | 5 |
pulmonary infiltrates | 5 |
major clinically | 5 |
low certainty | 5 |
result will | 5 |
screening will | 5 |
nebulised heparin | 5 |
samples obtained | 5 |
sargramostim will | 5 |
current proposed | 5 |
advisory unit | 5 |
respiratory morbidity | 5 |
vte events | 5 |
datasets used | 5 |
adult ae | 5 |
data review | 5 |
complement protein | 5 |
significant liver | 5 |
australian new | 5 |
medical events | 5 |
see additional | 5 |
therapeutic intervention | 5 |
plus inflammatory | 5 |
improve clinical | 5 |
gastrointestinal bleeding | 5 |
test center | 5 |
plus ciprofloxacin | 5 |
stem cells | 5 |
specialized covid | 5 |
major trauma | 5 |
patients showing | 5 |
septic shock | 5 |
dental pulp | 5 |
following information | 5 |
initiate iv | 5 |
methylprednisolone mg | 5 |
study alxn | 5 |
oxygen concentration | 5 |
chronic health | 5 |
antihypertensive medications | 5 |
positive effect | 5 |
european countries | 5 |
will quantify | 5 |
laboratory confirmation | 5 |
acute coronary | 5 |
carbon dioxide | 5 |
rising sharply | 5 |
assessment will | 5 |
applicable product | 5 |
placebo will | 5 |
health authorities | 5 |
preterm neonates | 5 |
participate will | 5 |
vous totalement | 5 |
probable case | 5 |
two consecutive | 5 |
alveolar proteinosis | 5 |
treatment arms | 5 |
sided significance | 5 |
improving oxygenation | 5 |
efficacy data | 5 |
sur les | 5 |
heterosexual intercourse | 5 |
local intranasal | 5 |
hospital within | 5 |
stroke onset | 5 |
electronic patient | 5 |
quintet recruitment | 5 |
th stage | 5 |
least points | 5 |
information card | 5 |
sans signes | 5 |
immune cells | 5 |
infectious complications | 5 |
severity score | 5 |
group randomised | 5 |
induced coagulopathy | 5 |
chief investigator | 5 |
flow chart | 5 |
traumatic brain | 5 |
significant disability | 5 |
itt analysis | 5 |
study findings | 5 |
patients receive | 5 |
icu ward | 5 |
lung tissue | 5 |
necrosis factor | 5 |
medical university | 5 |
medical doctor | 5 |
consent must | 4 |
mycoplasma pneumoniae | 4 |
secondary school | 4 |
potentially eligible | 4 |
alternative pathway | 4 |
closest study | 4 |
blood gases | 4 |
thrombotic complications | 4 |
document will | 4 |
ray index | 4 |
risk patients | 4 |
national institutional | 4 |
fair comparison | 4 |
trial findings | 4 |
city blocks | 4 |
epidemic period | 4 |
wei bushen | 4 |
additional weeks | 4 |
hydroxychloroquine treatment | 4 |
hospital wards | 4 |
nasal outcome | 4 |
mortality will | 4 |
less likely | 4 |
resolution computed | 4 |
data analyses | 4 |
transcutaneous co | 4 |
computer software | 4 |
project group | 4 |
stratification variables | 4 |
fifth affiliated | 4 |
working group | 4 |
dans cette | 4 |
odoratest jours | 4 |
ipm will | 4 |
average volume | 4 |
fio fraction | 4 |
highly suspect | 4 |
confounding factors | 4 |
existing tube | 4 |
covid infection | 4 |
research projects | 4 |
every visit | 4 |
acute illness | 4 |
healthy eating | 4 |
may choose | 4 |
related complications | 4 |
point prevalence | 4 |
positive pregnancy | 4 |
aedes control | 4 |
local pi | 4 |
interventional studies | 4 |
first laboratory | 4 |
datasets generated | 4 |
causality assessment | 4 |
acute myocardial | 4 |
detect sars | 4 |
control trials | 4 |
influenza infection | 4 |
dengue vector | 4 |
electronic randomization | 4 |
air quality | 4 |
beneficial effect | 4 |
mononuclear cells | 4 |
monocyte chemoattractant | 4 |
following awareness | 4 |
sputum samples | 4 |
rass goal | 4 |
determination via | 4 |
reports will | 4 |
timely manner | 4 |
blind randomized | 4 |
coordinating investigators | 4 |
plus corticosteroids | 4 |
collaborative care | 4 |
new protocol | 4 |
saudi food | 4 |
detailed description | 4 |
therapeutic target | 4 |
significantly affect | 4 |
intervention trial | 4 |
early stages | 4 |
recombinant human | 4 |
resource use | 4 |
relative stress | 4 |
trial coordination | 4 |
blood cultures | 4 |
short form | 4 |
lower airway | 4 |
formulas plus | 4 |
symptoms compatible | 4 |
international meetings | 4 |
asking questions | 4 |
apache ii | 4 |
causative agent | 4 |
authors acknowledge | 4 |
urgently needed | 4 |
drug related | 4 |
life questionnaire | 4 |
soc medication | 4 |
les autres | 4 |
ensure data | 4 |
newly diagnosed | 4 |
cure soft | 4 |
mental state | 4 |
receive ravulizumab | 4 |
many cases | 4 |
pradeesh sivapalan | 4 |
residual insecticide | 4 |
safety purposes | 4 |
premature termination | 4 |
regarding concomitant | 4 |
rheumatic diseases | 4 |
prospective cohort | 4 |
arterial puncture | 4 |
subject identification | 4 |
times per | 4 |
clinically important | 4 |
commercially available | 4 |
significant changes | 4 |
dose systemic | 4 |
experimental arms | 4 |
subcutaneous injection | 4 |
meier curves | 4 |
tous les | 4 |
low tidal | 4 |
examination will | 4 |
chaque centre | 4 |
ards according | 4 |
allow us | 4 |
test olfactif | 4 |
person will | 4 |
peripheral sensory | 4 |
requiring initiation | 4 |
haenszel test | 4 |
sign icf | 4 |
complex intervention | 4 |
receiving satisfying | 4 |
decisions regarding | 4 |
ensure confidentiality | 4 |
first icu | 4 |
dual antiplatelet | 4 |
antibiotic prophylaxis | 4 |
cord injury | 4 |
activity questionnaire | 4 |
taking place | 4 |
placebo capsules | 4 |
protection agency | 4 |
international conferences | 4 |
monitoring inspection | 4 |
noninferiority margins | 4 |
telemedicine technologies | 4 |
sur un | 4 |
detect differences | 4 |
first months | 4 |
start date | 4 |
paper handling | 4 |
use will | 4 |
improvement ordinal | 4 |
elizabeth hospital | 4 |
therapeutic strategy | 4 |
event meets | 4 |
daily measurements | 4 |
ritonavir treatment | 4 |
bp mmhg | 4 |
several hours | 4 |
please refer | 4 |
belgian law | 4 |
bacterial infection | 4 |
study report | 4 |
life years | 4 |
mean duration | 4 |
may increase | 4 |
beyond day | 4 |
performed within | 4 |
rapid diagnostic | 4 |
another study | 4 |
ciprofloxacin alone | 4 |
care plan | 4 |
leukocyte formula | 4 |
two major | 4 |
blinded outcome | 4 |
immune cell | 4 |
alveolar space | 4 |
whether treatment | 4 |
dose enoxaparin | 4 |
ctcae version | 4 |
national guidelines | 4 |
using mixed | 4 |
serious allergic | 4 |
ae ratings | 4 |
study enrollment | 4 |
providers including | 4 |
thrice daily | 4 |
patient population | 4 |
bp monitor | 4 |
experience suggests | 4 |
term follow | 4 |
terminated early | 4 |
alpha error | 4 |
routine blood | 4 |
group without | 4 |
muscle atrophy | 4 |
data entered | 4 |
stopping boundaries | 4 |
existing data | 4 |
data suggest | 4 |
support health | 4 |
medical costs | 4 |
local policies | 4 |
consecutive blood | 4 |
prior lung | 4 |
urban areas | 4 |
au cpp | 4 |
du juin | 4 |
disability incapacity | 4 |
cancer australia | 4 |
nv rhinospirometer | 4 |
human movement | 4 |
blood cytokine | 4 |
random effect | 4 |
surgical arm | 4 |
uncontrolled hypertension | 4 |
effect will | 4 |
categorical data | 4 |
two treatment | 4 |
investigator within | 4 |
young people | 4 |
detailed information | 4 |
edc system | 4 |
thilo trial | 4 |
variance estimator | 4 |
coordinating principle | 4 |
prophylactic treatment | 4 |
multiple comparisons | 4 |
authorities will | 4 |
study personal | 4 |
inspiratory pressure | 4 |
pour le | 4 |
multiple organ | 4 |
secondary clinical | 4 |
le test | 4 |
heart valve | 4 |
final assessment | 4 |
patients meeting | 4 |
scientific committee | 4 |
therapeutics inc | 4 |
based study | 4 |
risk benefit | 4 |
previous study | 4 |
type ii | 4 |
test stratified | 4 |
table will | 4 |
without sarilumab | 4 |
date data | 4 |
des documents | 4 |
study start | 4 |
pronostic vital | 4 |
experimental treatment | 4 |
direct oral | 4 |
ctcae toxicities | 4 |
following reasons | 4 |
leur sera | 4 |
also known | 4 |
dementia plan | 4 |
outcomes listed | 4 |
disease study | 4 |
envelope method | 4 |
dosage regimen | 4 |
effectively inhibit | 4 |
patient file | 4 |
thromboembolic disease | 4 |
two weeks | 4 |
acute lower | 4 |
enoxaparin injections | 4 |
third season | 4 |
subject number | 4 |
clinical chemistry | 4 |
saline solution | 4 |
peep selected | 4 |
fatal saes | 4 |
will proceed | 4 |
average red | 4 |
graphpad prism | 4 |
symptoms may | 4 |
early termination | 4 |
trial completion | 4 |
systemic steroids | 4 |
biomedical research | 4 |
plague season | 4 |
icu days | 4 |
used will | 4 |
parallel control | 4 |
study set | 4 |
deviations will | 4 |
fourfold increase | 4 |
sequentially numbered | 4 |
patients du | 4 |
proposed study | 4 |
disease caused | 4 |
aes saes | 4 |
signes respiratoires | 4 |
nasal cavity | 4 |
sharing platform | 4 |
cantonal hospitals | 4 |
existing condition | 4 |
handicap inventory | 4 |
randomization procedure | 4 |
time without | 4 |
via arterial | 4 |
proposed intervention | 4 |
significant risk | 4 |
will show | 4 |
annual safety | 4 |
versus placebo | 4 |
huang qin | 4 |
blood oxygenation | 4 |
entourez une | 4 |
documentation will | 4 |
injection site | 4 |
must provide | 4 |
antibody titre | 4 |
induced acute | 4 |
positive samples | 4 |
expanded access | 4 |
intervention components | 4 |
acute onset | 4 |
weight adjusted | 4 |
contralateral turbinate | 4 |
also shown | 4 |
interquartile ranges | 4 |
restoring lung | 4 |
common respiratory | 4 |
ventilator will | 4 |
ferritin levels | 4 |
injury induced | 4 |
les traitements | 4 |
drug authority | 4 |
based care | 4 |
examination findings | 4 |
fois par | 4 |
received sufficient | 4 |
one study | 4 |
generated random | 4 |
prospective study | 4 |
lung oxygenation | 4 |
outcome assessor | 4 |
high mortality | 4 |
related aes | 4 |
secondary bacterial | 4 |
le virus | 4 |
peep titration | 4 |
receive anakinra | 4 |
active smoker | 4 |
research associates | 4 |
may contribute | 4 |
hospital zurich | 4 |
ordinal score | 4 |
measuring blood | 4 |
respiratory drive | 4 |
systemic cytokine | 4 |
important difference | 4 |
takes place | 4 |
will explore | 4 |
comparisons will | 4 |
early application | 4 |
received research | 4 |
health science | 4 |
ou non | 4 |
des produits | 4 |
investigator site | 4 |
lower peep | 4 |
day visits | 4 |
equivalent cs | 4 |
nasal septoplasty | 4 |