All participants
[용어속성] Patient
Perceived Effectiveness, Safety, and Attitudes Toward the Use of Nucleic Tests of SARS-CoV-2 Among Clinicians and General Public in China
중국의 임상의와 일반 대중 사이에서 SARS-CoV-2의 핵 검사 사용에 대한 인식된 효과, 안전성 및 태도
Public Health
[키워드] Accuracy
acute respiratory syndrome
acute respiratory syndrome coronavirus
acute respiratory syndrome coronavirus 2
All participant
All participants
approval
Attitude
biomedicine
China
Chinese
Compliance
conducted
coronavirus
coronavirus disease
Coronavirus disease 2019
Coverage
COVID-19
cross-sectional
cross-sectional study
Efficacy
Epidemic
female
IMPROVE
knowledge
Likert scale
majority
Novel coronavirus
nucleic test
pandemic
participant
Perceived
positive
positive attitude
Public
questionnaire
recruited
Research
research and development
respiratory
Safety
SARS-CoV-2
SARS-CoV-2 virus
severe acute respiratory syndrome Coronavirus
tension
Test
test kits
the SARS-CoV-2 virus
was obtained
were measured
[DOI] 10.3389/fpubh.2020.599862 PMC 바로가기 [Article Type] Public Health
[DOI] 10.3389/fpubh.2020.599862 PMC 바로가기 [Article Type] Public Health
Nebulised surfactant for the treatment of severe COVID-19 in adults (COV-Surf): A structured summary of a study protocol for a randomized controlled trial
성인의 중증 COVID-19 치료를 위한 분무형 계면활성제(COV-Surf): 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Randomized Controlled Trial
[키워드] 1080
24 hour
24 hours
48 hour
48 hours
ACE2
ADEs
administration
Adverse
adverse event
adverse events
AEs
ALEA
All participant
All participants
allergy
alveolar
angiotensin
angiotensin converting enzyme
angiotensin converting enzyme 2
anticipated
attending physician
bind
Blinding
block randomization
Blood
bovine
breath
buffer
calcium
cells
cellular
cholesterol
Chronic kidney disease
class
clinical
Clinical improvement
clinical trial
clinical trials
Cohort
Combination
comparator
Compliance
Concentration
conducted
Consent
contraindication
contributing to
Control
control arm
controls
COVID-19
COVID-19 adult patient
COVID-19 patients
current
cytokine
Data collection
Data monitoring committee
death
declined
defined
delivery
described
Device
dialysis
discretion
dissemination
dose
drug
Effect
Efficacy
EGFR
element
Eligible participants
end point
End-Expiratory Pressure
Endotracheal intubation
enrolled
Enrollment
enrolment
epithelial
Escalation
EudraCT
evaluate
exclusion
exclusion criteria
expected
fatty
Fatty acid
feasibility
free fatty acid
Frequency
hospital
hospitalised
hypoxia
impair
include
inclusion criteria
index
Inflammatory marker
inflammatory markers
Inflammatory response
intensive care
intensive care unit
Intervention
investigator
Kidney disease
lack
liver
liver failure
Local
lung
lung lavage
mechanical ventilation
mechanical ventilator
mechanically ventilated patient
mechanically ventilated patients
mixture
Mortality
nebulisation
number
objective
Open-label
opinion
Ordinal Scale
other treatment
outcome
oxidative stress
Oxygenation
PaO
participant
Patient
PCR
PEEP
Phosphatidylcholine
phosphatidylethanolamine
phosphatidylglycerol
phosphatidylinositol
phospholipid
PIP
Placebo
plasma
Pneumothorax
Positive end-expiratory pressure
Prevent
Primary outcome
progression
Protein
protocol
pulmonary compliance
pulmonary hemorrhage
pulmonary ventilation
quantification
randomisation
randomised
randomised controlled trial
Randomized
Randomized controlled trial
reached
receive
recorded
recruitment
reduction
Registered
reported
Respiratory failure
SAEs
Sample size
SARS-CoV-2 viral load
SARS-CoV-2 virus
secondary outcome
Secondary outcomes
Serious Adverse Events
severe COVID-19
severity
sphingomyelin
Stage
Standard
Standard of care
status
Study protocol
subject
supplementary material
surface tension
surfactant
synthesis
tension
the WHO
tissue damage
total sample size
tracheal
tracheal aspirate
Tracheal aspirates
transfer
Treatment
Trial
Trial Steering Committee
turnover
unique
university
University College London
usual standard of care
Ventilation
Ventilation Index
ventilatory support
VFD
vibrating mesh nebulizer
Viral
Viral load
virus
water
website
weight
with COVID-19
worsening
[DOI] 10.1186/s13063-020-04944-5 PMC 바로가기 [Article Type] Randomized Controlled Trial
[DOI] 10.1186/s13063-020-04944-5 PMC 바로가기 [Article Type] Randomized Controlled Trial
6-month SARS-CoV-2 antibody persistency in a Tyrolian COVID-19 cohort
티롤리안 COVID-19 코호트에서 6개월 SARS-CoV-2 항체 지속성
Original Article
[키워드] acute respiratory syndrome
acute respiratory syndrome coronavirus
age
All participant
All participants
Anti-viral
anti-viral antibody
antibody
antibody response against
Antibody testing
Arthritis
average
binding antibody
caused
convalescent
coronavirus
coronavirus disease
Coronavirus disease 2019
COVID-19 cohort
cut-off
cut-off point
decrease
Diagnosis
disease
disease onset
dropped
ELISA
except for
Follow-up
healthy
Hyposmia
identify
Immunity
immunized
individuals
Infection
information
life
Neutralizing
Neutralizing antibodies
neutralizing antibody
participant
Prospective
Receptor binding domain
respiratory
Result
rheumatoid arthritis
S1 subunit
SARS-CoV-2 antibody
severe acute respiratory syndrome Coronavirus
specificity
Spike protein
the S1 subunit
the spike protein
titers
virus
were used
[DOI] 10.1007/s00508-020-01795-7 PMC 바로가기 [Article Type] Original Article
[DOI] 10.1007/s00508-020-01795-7 PMC 바로가기 [Article Type] Original Article
Human Leukocyte Antigen Complex and Other Immunogenetic and Clinical Factors Influence Susceptibility or Protection to SARS-CoV-2 Infection and Severity of the Disease Course. The Sardinian Experience
인간 백혈구 항원 복합체 및 기타 면역유전학적 및 임상적 요인은 SARS-CoV-2 감염에 대한 감수성 또는 보호 및 질병 경과의 중증도에 영향을 미칩니다. 사르데냐 체험
Randomized Controlled Trial
[키워드] 95% CI
All participants
allele
alleles
analyzed
Asymptomatic
asymptomatic or pauci-symptomatic patients
Autoimmune disease
Autoimmune diseases
beta-thalassemia
beta-thalassemia trait
beta-thalassemic trait
Care
carried
clinical
Clinical data
Clinical outcome
clinical, genetic and immunogenetic factors
collected
controls
Course
COVID-19 severity
deficiency
Demographic and clinical data
disease course
DRB1
evaluate
experience
extended haplotype
Factor
Frequency
G6PDH
G6PDH deficiency
Genetic
genetic factor
genetic factors
Genetic polymorphism
Glucose
Glucose-6-phosphate
glucose-6-phosphate dehydrogenase
haplotype frequencies
haplotypes
health problem
healthy
HLA allele
HLA class I
HLA class I and II molecules
HLA-A
HLA-A*02:05, B*58:01, C*07:01
HLA-A*30:02
HLA-A*30:02, B*14:02, C*08:02
HLA-C
HLA-C*04:01 allele
HLA-DRB1*08:01 allele
home care
home care patients
hospital
hospital care
hospitalized patient
hospitalized patients
Human
human leukocyte antigen
immunogenetic background
immunogenetic factors
in-patient
infections
influence
Influenza
influenza vaccination
Italy
Male sex
material
Mild disease
negative influence
Older age
Other
Participants
Pathogenesis
Patient
patients
pauci-symptomatic
phosphate
predisposing factor
protection
protective effect
public health
recruited
related clinical consequence
related clinical consequences
required
Result
Sardinia
Sardinian
Sardinian control
Sardinian population
SARS-CoV-2
SARS-COV-2 infection
SARS-CoV-2 patients
seasonal flu
severe disease
Sex
susceptibility
Taking
thalassemia
the disease
three-loci haplotype
vaccination
with mild disease
without symptoms
world-wide public health problem
[DOI] 10.3389/fimmu.2020.605688 PMC 바로가기 [Article Type] Randomized Controlled Trial
[DOI] 10.3389/fimmu.2020.605688 PMC 바로가기 [Article Type] Randomized Controlled Trial
The effect of propolis supplementation on clinical symptoms in patients with coronavirus (COVID-19): A structured summary of a study protocol for a randomised controlled trial
코로나바이러스(COVID-19) 환자의 임상 증상에 대한 프로폴리스 보충제의 효과: 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Randomized Controlled Trial
[키워드] 1:1
age
All participants
anticipated
Arm
baseline
Blinding
block size
calculated
categories
Cellulose
changes in
clinical
clinical symptom
Clinical symptoms
Clinicians
color
concealed
control group
coronavirus
coronavirus disease
COVID-19
Date
dissemination
double-blind
element
eligible
hospital
Intervention
intervention group
investigator
investigators
Iran
labelling
microcrystalline
microcrystalline cellulose
name
number
objective
odor
outcome
Parallel Arm
participant
Participants
Patient
patients
PCR test
performed
pharmaceutical
phase
Placebo
placebo-controlled clinical trial
Propolis
protocol
Protocol study
provided
randomised controlled trial
randomization
randomization list
randomization sequence
Randomized
Randomly
receive
recruited
Registered
registration number
Reyhan
Sample size
sealed
sensitivity
sequence
severity
Sex
shape
stratified
Study protocol
supplementary material
Tablet
Taste
total sample size
Trial
Trial registration
Version
Warfarin
website
weight
[DOI] 10.1186/s13063-020-04934-7 PMC 바로가기 [Article Type] Randomized Controlled Trial
[DOI] 10.1186/s13063-020-04934-7 PMC 바로가기 [Article Type] Randomized Controlled Trial
Is older age associated with COVID-19 mortality in the absence of other risk factors? General population cohort study of 470,034 participants
다른 위험 요소가 없는 경우 고령이 COVID-19 사망률과 관련이 있습니까? 470,034명의 참가자를 대상으로 한 일반 인구 코호트 연구
Research Article
[키워드] 95% CI
absence
age
All participants
association
baseline
baseline data
cohort study
COVID-19
COVID-19 mortality
current
deaths
died
Eligible participants
expiratory
explained
Factor
forced expiratory volume
high systolic blood pressure
higher risk
increased mortality
independent risk factor
Low forced expiratory volume
low handgrip strength
mediators
Mortality
mortality risk
much lower
multiple long-term condition
multiple long-term conditions
Older
Older adults
Older age
participant
Participants
Poisson regression
reported
Result
risk
risk factor
Risk factors
Systolic blood pressure
UK biobank
Volume
was used
with COVID-19
[DOI] 10.1371/journal.pone.0241824 PMC 바로가기 [Article Type] Research Article
[DOI] 10.1371/journal.pone.0241824 PMC 바로가기 [Article Type] Research Article
The Efficacy of Famotidine in improvement of outcomes in Hospitalized COVID-19 Patients: A structured summary of a study protocol for a randomised controlled trial
입원한 COVID-19 환자의 결과 개선에 대한 파모티딘의 효능: 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Letter
[키워드] Alanine
Alanine transaminase
alcoholism
All participant
All participants
allergies
allergy
allocation
approved
ARMS
aspartate
Aspartate transaminase
assigned
assumption
Bandar Abba
Bandar Abbas
baseline
Blinding
block randomization
blood count
Care
Chronic kidney disease
clearance
clinical
clinical trial
clinical trials
code
Committee
company
comparator
Comparator group
complete blood count
concealed
control group
control groups
COVID-19
COVID-19 patient
COVID-19 patients
creatinine
creatinine clearance
criteria
Dasatinib
dialysis
discharge
dissemination
dosage
drug therapy
electrocardiogram
element
eligibility criteria
End-stage renal disease
ethics committee
Evidence
evidence of
excluded
expected
Famotidine
G6PD
Glucose
Glucose 6 phosphate
grouping
groups
Hepatitis
hepatitis C
Hospitalized
Immunocompromised
Immunocompromised patients
Infection
Intervention
Kidney disease
Lactate
lactate dehydrogenase
lead
limit
Liver disease
Local
lung infiltration
maximum
Medical Science
Medical Sciences
moderate
need for dialysis
Neratinib
normal limit
number
objective
online tool
oral contraceptives
outcome
outcome assessor
outcome assessors
oxygen
oxygen saturation
Ozanimod
participant
Patient
patients
patients with COVID-19
Pazopanib
PCR test
pharmaceutical
Pharmaceutical Company
phosphate
Placebo
placebo-controlled
porphyria
positive
Pregnancy
protocol
psoriasis
random
randomisation
randomised
randomised controlled trial
randomized clinical trial
Randomly
randomly divided
receive
recruitment
Registered
registry
renal
renal disease
renal failure
reported
Research question
researcher
respiration rate
responsible
Rilpivirine
Sample size
sample size calculation
sequence
sequence information
single-blind
Siponimod
Standard
study drug
Study protocol
subject
submitted
technology
temperature
the ethics committee
therapy
title
Tizanidine
transaminase
Treatment
treatment group
Treatment protocol
treatment protocols
Trial registration
two group
two groups
university
Version
website
were measured
written consent
[DOI] 10.1186/s13063-020-04773-6 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04773-6 PMC 바로가기 [Article Type] Letter
Safety and immunogenicity of two heterologous HIV vaccine regimens in healthy, HIV-uninfected adults (TRAVERSE): a randomised, parallel-group, placebo-controlled, double-blind, phase 1/2a study
HIV에 감염되지 않은 건강한 성인을 대상으로 한 두 가지 이종 HIV 백신 요법의 안전성 및 면역원성(TRAVERSE): 무작위 배정, 병렬 그룹, 위약 대조, 이중 맹검, 1/2a상 연구
Articles
[키워드] 95% CI
Ad26
Adenovirus
Administered
advancement
adverse event
adverse events
aligned
All participant
All participants
Analysis
Antigen
antigens
applied
assigned
binding antibodies
binding antibody
blood sample
breadth
CD4+ T-cell
clade
collected
computer-generated
Defense
Deltoid muscle
Department
diagnosed
dose
double-blind
Efficacy
elicit
Eligible participants
ELISpot responses
enrolled
finding
first vaccination
foundation
funding
group
groups
healthy
Heterologous
HIV
HIV infection
HIV vaccine
HIV-1 infection
HIV-uninfected
IFNγ ELISPOT response
IFNγ ELISPOT responses
IgG
immune response
immune responses
Immunity
immunogenicity
injection
Intramuscular injection
investigator
investigators
Jackson
janssen
Laboratory
Local
magnitude
median
medical history
Medicine
Melinda Gate
Melinda Gates
Military Medicine
mononuclear cell
mononuclear cells
opinion
Other
parallel-group
participant
PBMC
PBMCs
per protocol
per-protocol
Peripheral blood
Peripheral blood mononuclear cells
Physical examination
Placebo
placebo group
placebo-controlled
placebos
prevention
randomisation
randomised
Randomly
randomly permuted block
randomly permuted blocks
regimen
regimens
Registered
repeated
risk
Safe
Safety
second vaccination
Sponsor
stratified
subgroups
systemic reactogenicity
T-cell Response
tested
tetravalent
the placebo group
titre
titres
Tolerability
treatment allocation
Trial
trivalent
USA
vaccination
vaccination schedule
Vaccinations
Vaccine
vaccine group
vectored vaccine
vital sign
was done
with HIV
[DOI] 10.1016/S2352-3018(20)30229-0 PMC 바로가기 [Article Type] Articles
[DOI] 10.1016/S2352-3018(20)30229-0 PMC 바로가기 [Article Type] Articles
Effect of an E-Learning Module on Personal Protective Equipment Proficiency Among Prehospital Personnel: Web-Based Randomized Controlled Trial
병원 전 직원의 개인 보호 장비 숙련도에 대한 E-Learning 모듈의 효과: 웹 기반 무작위 대조 시험
Original Paper
[키워드] added
All participant
All participants
baseline
both groups
Care
communication
confidence
Contamination
control group
Controlled
coronavirus
coronavirus disease
COVID-19
demonstration
donning sequence
e-learning group
e-learning module
Effect
effective
effective communication
electronic learning
eligible
email
equipment
evaluate
for inclusion
gamified
gamified e-learning module
groups
Health
Health care
IMPROVE
in both group
infection control
Infection control guidelines
Intervention
investigators
IQR
knowledge
misuse
module
no significant difference
objective
online learning
outcome assessors
pandemic
participant
Participants
Personal protective equipment
PPE
prehospital
preintervention
proportion
protection
Randomized
Randomized controlled trial
Result
risk
Safety
second set
shown
significantly
statistically significant
Switzerland
the median
Trial
web-based study
Work environment
[DOI] 10.2196/21265 PMC 바로가기 [Article Type] Original Paper
[DOI] 10.2196/21265 PMC 바로가기 [Article Type] Original Paper