accompany
[용어속성] Term
The effect of surfactant on clinical outcome of patients with COVID-19 under mechanical ventilation: A structured summary of a study protocol for a randomised controlled trial
Letter
[키워드] 1:1
6 hour
accompany
acute respiratory distress syndrome
addition
adjusted
Administered
age
anticipated
approach
ARDS
Assessing
auxiliary
Bacterial
blinded
Care
Clinical outcome
control group
COVID-10
COVID-19
COVID-19 patient
discharge
disease
dissemination
dose
doses
ECMO
element
etiology
Existence
extracorporeal membrane oxygenation
Face mask
Healthcare provider
hospital
hospital discharge rate Randomised controlled trial
Hospital length of stay
ICU
information
intervention group
intubation
investigator
Iran
less
lung involvement
mechanical ventilation
moderate
Mortality
much lower
number
objective
outcome
P/F ratio
parallel group
participant
Patient
patient mortality
patients with COVID-19
Pneumonia
protocol
pulmonary disease
pulmonary involvement
random
randomisation
randomised
randomised controlled trial
receive
Registration
researchers
Sample size
SARS-CoV-2
second dose
sequence
severe ARDS
status
Study protocol
surfactant
Tehran
the patient
time
Trial
ventilator
Version
Volume
website
written consent
[DOI] 10.1186/s13063-020-04815-z PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04815-z PMC 바로가기 [Article Type] Letter
Neuropathobiology of COVID-19: The Role for Glia
Cellular Neuroscience
[키워드] accompany
adaptive
Affect
Ageing
angiotensin-converting enzyme 2
Astrocyte
Autoimmunity
binding
Brain
cause
cells
chemokine
circulating
Comorbidities
Comorbidity
consequence
COVID-19
Critical
development
expressed
Foetus
function
Health
homeostatic
immune
Immune cell
Immunity
increase in
Inflammatory mediators
Innate immunity
microglia
microglial
mother
Neuroinflammation
neurological
organ
outcome
pandemic
pregnant
Psychiatric
receptor
required
role
SARS-CoV-2
SARS-COV-2 infection
Severe case
systemic infection
Trigger
[DOI] 10.3389/fncel.2020.592214 PMC 바로가기 [Article Type] Cellular Neuroscience
[DOI] 10.3389/fncel.2020.592214 PMC 바로가기 [Article Type] Cellular Neuroscience
Hyperimmune anti-COVID-19 IVIG (C-IVIG) Therapy for Passive Immunization of Severe and Critically Ill COVID-19 Patients: A structured summary of a study protocol for a randomised controlled trial
Letter
[키워드] 28-day mortality
accompany
acute lung injury
adverse event
airway
All participant
allergic
anti-COVID19 IVIG
Anti-viral
Antibiotics
assigned
assisted ventilation
autoimmune disorder
blinded
Blood oxygen saturation
blood pressure
C-IVIG
Care
Clinical efficacy
Comparator group
convalescent plasma
COVID-19
COVID19
criteria
Critically ill
Critically ill patient
CRP
current
disorder
dosage
Dyspnea
excluded
Follow-up
four group
group
hemodynamic
hemolytic anemia
hospital
hospital discharge
Hospital stay
hypersensitivity
ICU
IgA deficiency
Ill
immunization
Immunoglobulin
include
infected individual
Inflammation
information
inotropic agent
Intervention
intervention arm
Isolation
Karachi
kidney
Kidney failure
lung infiltrate
maintain
Manifestations
medication
Meningitis
MONITOR
multiple organ dysfunction
nasopharyngeal
neutrophil lymphocyte ratio
number
objective
observé
oropharyngeal swabs
outcome
PaO
parallel-group
participant
Passive
passive immunization
Patient
patients
positive SARS-CoV-2 PCR
pregnant females
Primary outcome
protocol
randomised
randomised controlled
randomised controlled trial
randomization
receive
recruited
Registered
reported
Respiratory failure
respiratory rate
Sample size
sealed
Septic shock
shifting
single dose
standard care
status
Steroids
Study protocol
Support
symptoms of COVID-19
therapy
thromboembolic
Total
Treatment
Trial
university
website
were excluded
with COVID-19
[DOI] 10.1186/s13063-020-04839-5 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04839-5 PMC 바로가기 [Article Type] Letter
A Trial of Favipiravir and Hydroxychloroquine combination in Adults Hospitalized with moderate and severe Covid-19: A structured summary of a study protocol for a randomised controlled trial
Letter
[키워드] 1:1
accompany
adjusted
Admission
Affair
age
analyst
antibiotic
antiviral therapy
Arrhythmias
blinded
Breastfeeding
breathing ambient air
Care
Child-Pugh score
Chronic kidney disease
city
classical
clinical
clinical effectiveness
Clinical improvement
clinical sample
clinical symptom
clinically
Coma
Combination
Comorbidity
comparator
Compliance
conducted
control arm
control group
Controlled clinical trial
COVID-19
current
Dammam
data entry
death
deficiency
defined
diagnosed with COVID-19
dialysis
discharge
discharged
disease
disease onset
dissemination
drug
ECMO
effective sample size
Efficacy
Efficacy and safety
eight
element
enrolled
Enrollment
evaluate
Evidence
experimental arm
extracorporeal membrane oxygenation
Faisal
Favipiravir
female
G6PD
Glucose-6-phosphate
hereditary xanthinuria
HIV
hospital
Hospital admission
Hospitalized
Hydroxychloroquine
Hyperuricemia
ICU admission
Imam
immunosuppressive
in vitro
include
information
Intervention
intravenous fluid
invasive ventilation
investigator
Jeddah
King
less
limit
Liver damage
Major
malignancy
medication
moderate
multicenter
Multicenter trial
Myocardial infarction
noninvasive
nonpregnant
number
objective
ongoing trial
outcome
oxygen saturation
Palliative care
participant
Patient
PCR
pregnant
primary endpoint
prior diagnosis
prognostic
prolonged QT interval
protocol
QT interval
randomised
randomised controlled trial
randomization
Randomized
receiving
recruitment
reference
risk
Sample size
SARS-CoV-2
Saudi Arabia
selected
seven-category ordinal scale
Standard
Stratification
study drug
Study protocol
subject
supplemental oxygen
Supportive treatment
Symptom
System
tablets
the patient
therapeutic agent
therapy
transferred
Treatment
Trial
ULN
Urinary tract
use of hydroxychloroquine
vasopressor support
ventricular
viral infection
Web
website
with COVID-19
xanthine
[DOI] 10.1186/s13063-020-04825-x PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04825-x PMC 바로가기 [Article Type] Letter
nSARS-Cov-2, pulmonary edema and thrombosis: possible molecular insights using miRNA-gene circuits in regulatory networks
Research
[키워드] accompany
Antigen presentation
antigen-presentation
approach
Cell
coronavirus 2
Diseases
disorder
drugs
edema
Factor
Features
Feed forward loops
FFLs
identify
Infection
Inflammatory response
information
loop
miRNA
miRNA coregulatory networks
molecular
molecular mechanism
motif
nSARS-CoV-2
pandemic
pathophysiology
pathway
pulmonary disease
Pulmonary edema
regulate
regulatory circuit
regulatory network
Research
respiratory
Result
Signaling
signaling pathway
signaling pathways
similarity
Spread
symptomatic
targets
TGF
the disease
thromboembolic
thrombosis
trajectory
unique
vaccine candidate
viral replication
virus
virus spike protein
while
[DOI] 10.1186/s41544-020-00057-y PMC 바로가기 [Article Type] Research
[DOI] 10.1186/s41544-020-00057-y PMC 바로가기 [Article Type] Research
Safety and Efficacy of Imatinib for Hospitalized Adults with COVID-19: A structured summary of a study protocol for a randomised controlled trial
Letter
[키워드] 1:1
24 hour
Ability
absence
accompany
activity
Administered
administration
Admission
adverse events
Affect
age
alkaline phosphatase
allergy
ALT
alternative hypothesis
ambient
Analysis
ANC
Anti-inflammatory
anticipated
antipyretics
antivirals
Arm
ARMS
assumed
AST
Baltimore
baseline
benefit
blinded
block
block randomization
Blood
breastfeeding women
Bronchoalveolar lavage
calculated
Care
Cellulose
center
Chest
chest X-ray
childbearing potential
clinical
clinical condition
Clinical course
clinical impact
Clinical improvement
Clinical outcome
clinical status
clinical trial
collected
competing
Compliance
concealed
Concentration
Concomitant
conditions
conducted
congestive heart failure
Contraception
Control
control arm
Conventional
Corticosteroids
COVID-19
COVID-19 disease
COVID-19 infection
COVID-19 pandemic
criteria
criterion
Critical
CT scan
current
Day
Declaration of Helsinki
decrease
defined
detect
direct bilirubin
disease
disorder
dissemination
dose
double-blind
drug
Drug administration
drug-drug interaction
drugs
Duration
ECMO
Efficacy
Efficacy and safety
element
eligible
endosomal pH
Enrollment
ethnic group
evaluate
Evidence
exclusion
expected
exploratory endpoint
extracorporeal membrane oxygenation
Face mask
FDA
Fisher
Good
group
handling
harmonization
hematologic
histocompatibility complex
Hospitalization
Hospitalized
hospitalized patient
Hydroxychloroquine
Hypothesis
ICU
IL-6 levels
Imatinib
immunomodulatory
immunomodulatory drugs
IND
information
Informed consent
inhibitory activity
intensive care
intensive care unit
intention to treat
interfere
International Conference
invasive
Invasive mechanical ventilation
investigational agent
investigator
ITT
Laboratory
Last
limit
limitation
liver
Local
lysosomal sequestration
magnitude
matching placebo
mechanical ventilation
men and women
MHC
mononuclear cell
Mortality
nasal
nasopharyngeal
Nasopharyngeal swab
neutrophil count
New
new oxygen use
non-invasive ventilation
non-rebreather mask
not blinded
null hypothesis
number
objective
off-label
off-label use
Oropharyngeal
outcome
outcomes
oxygen
Oxygenation
P450
packaged
PaO
participant
Participants
Patient
patients
patients with ARDS
patients with COVID-19
PBMCs
performed
Pharmacist
Pharmacy
phase 3 study
Placebo
placebo-controlled
Pneumonia
positive COVID-19
Practice
primary analysis
primary endpoint
principal
progression
proportion
protocol
Psychiatric
Radiographic
random number generator
randomised controlled trial
randomization
Randomized
Randomized controlled trial
receive
receiving
recruitment
Regulatory
renal dysfunction
renal replacement therapy
replication of SARS-CoV-2
required
requiring supplemental oxygen
Respiratory illness
respiratory tract
risk
RT-PCR
Safety
Sample size
sarilumab
SARS-CoV
SARS-CoV-2
secondary endpoint
Seizure
Serious Adverse Events
service
severe disease
severity
significance level
Site
Society
stability
Standard of care
status
stratified
study drug
study enrollment
study outcomes
Study protocol
subject
submitted
supplemental oxygen
Support
Suspension
symptomatic
Tablet
temperature
Test
the patient
the primary endpoint
time
TKI
TKI-induced attenuation of vascular leak
TKI-induced prevention and treatment lung inflammation
Tocilizumab
transcriptomics
Treatment
treatment allocation
treatment arm
treatments for COVID-19
Trial
two-sided
tyrosine kinase inhibitor
uncontrolled
university
unstable angina
vasopressors
ventilator
ventilator free days
viral ABL-1 signalling
website
with COVID-19
[DOI] 10.1186/s13063-020-04819-9 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04819-9 PMC 바로가기 [Article Type] Letter
The efficacy of Siddha Medicine, Kabasura Kudineer (KSK) compared to Vitamin C & Zinc (CZ) supplementation in the management of asymptomatic COVID-19 cases: A structured summary of a study protocol for a randomised controlled trial
Letter
[키워드] 1:1
accompany
addition
adverse effect
Asymptomatic
Asymptomatic COVID-19
baseline
blinded
breathlessness
bronchial asthma
calculated
carried
Chain Reaction
changes in
Chennai
clinical
clinical assessment
clinical trial
co-morbidity
college
control group
cough
COVID
COVID-19
CTRI
Data analysis
determine
Diabetes Mellitus
dissemination
dose
Efficacy
element
eligibility assessment
evaluate
excluded
exploratory
Factor
Fever
filtered
Herbal decoction
hypertension
IFNγ
IL10
IL2
Immunity
immunological
independent
India
information
investigator
involved
lactating
malignancy
management
marker
Medicine
Microsoft Excel
number
objective
Occurrence
onset of symptom
Open-label
outcome
parallel group
participant
positive
pregnant
Primary outcome
progression
protocol
random number generation
randomised
randomised controlled trial
randomization
Randomized controlled trial
receive
recruit
recruited
recruitment
reduced
reducing
reduction
reduction in
Registered
reported
RT-PCR
Sample
Sample size
SARS-CoV-2 viral load
sealed
Secondary outcomes
severe respiratory disease
Siddha
Siddha Medicine
Standard
state
Study protocol
submitted
Symptom
symptomatic
Tablet
tested
the SARS-CoV-2
threshold
TNF
traditional methods
Treatment
Trial
Tumor
Vitamin
website
Zinc
[DOI] 10.1186/s13063-020-04823-z PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04823-z PMC 바로가기 [Article Type] Letter
Assessment of boron-containing compounds and oleoylethanolamide supplementation on the recovery trend in patients with COVID-19: A structured summary of a study protocol for a randomized controlled trial
Letter
[키워드] 1:1
accompany
age
Antibody test
anticipated
assessment
assigned
blinded
block
Boron-containing compounds
Breastfeeding
C-reactive protein
C-reactive protein (CRP
calculated
CBC
center
clinical
Clinical symptoms
clinical trial
complete blood count
Compound
computer-generated
conducted
COVID-19
Critical
Data analysis
diagnosis of SARS-CoV-2
dissemination
double-blind
dry cough
element
erythrocyte sedimentation rate
ESR
exclusion criteria
fatigue
Features
female
Fever
four groups
group
groups
Imam
include
inclusion criteria
Infection
information
Intervention
investigator
Iran
male
Medical Sciences
number
nutrition
objective
Oleoylethanolamide
outcome
participant
Patient
patients
patients with COVID-19
PCR
placebo-controlled clinical trial
Pneumonia
polymerase chain
Pregnancy
primary end point
profile
protocol
randomised
randomised controlled trial
randomization
Randomized
Randomized controlled trial
Randomly
receive
Registered
registry
Reza
Sample size
single-center
status
Study protocol
subject
Tabriz
total sample size
Treatment
Trial
university
Version
website
[DOI] 10.1186/s13063-020-04820-2 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04820-2 PMC 바로가기 [Article Type] Letter
An investigation into the beneficial effects of high-dose interferon beta 1-a, compared to low-dose interferon beta 1-a (the base therapeutic regimen) in moderate to severe COVID-19: A structured summary of a study protocol for a randomized controlled l trial
Letter
[키워드] 1:1
accompany
Admission
age
alcohol
allocation concealment
ALT/AST
Arm
assigned
Beta
block-randomization
Blood
body temperature
Care
clinical
Clinical improvement
clinical trial
comparator
Confirmed
control group
COVID
COVID-19
COVID-2019
CT scan
death
discharge
disease
dissemination
drug
duration of hospitalization
Effect
Effectiveness
element
eligibility criteria
exclusion criteria
fatigue
group
headache
Health
High dose
High-dose
hospital
hospital discharge
Hospitalization
improvement
incidence
include
Infection
information
Interaction
interferon beta
Interferon beta-1a
Interferon-β 1a
intervention group
Intubated
Invasive mechanical ventilation
investigator
Kaletra
Laboratory results
lactating women
Last
less
limit
Loghman Hakim Hospital
Lopinavir/ritonavir
low dose
low-dose
masking
mechanical ventilation
Medical Sciences
moderate
Mortality
nasal
Non-invasive
number
objective
open label
Open-label
outcome
oxygen saturation
oxygen support
package
parallel group
participant
Patient
pregnant
Primary outcome
primary outcome measure
professional
protocol
R software
Radiation
randomised
randomization
randomization sequence
Randomized
Randomized controlled trial
Randomly
receive
Recigen
recruitment
refusal
regimen
Registered
Research
respiratory rate
Ritonavir
RT-PCR
RT-PCR test
Sample size
SARS-CoV-2
sealed
secondary
secondary outcome
seven-category ordinal scale
severe disease
Shortness of breath
single center
standard care
status
Study protocol
Symptom
the patient
therapeutic
time
treated
treatment groups
Trial
two groups
university
version 3.6.1
website
World Health Organization
[DOI] 10.1186/s13063-020-04812-2 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04812-2 PMC 바로가기 [Article Type] Letter