table
[용어속성] Term
Increased Productivity and Efficiency Among Cancer Center Clinical Trials Workforce during the COVID-19 Pandemic
Conference abstract
[키워드] A p-value
Analysis
analyzed
average
center
clinical
clinical trial
comparison
continuous variable
COVID-19
data entry
database
defined
disease
download
Efficiency
funding
greater
group
groups
hematology
Imago
include
increase in
Increased
Incyte
independent of
interquartile range
IQR
leukemia
logistic regression model
median
median time
Multiple myeloma
no significant difference
observation
organizations
pandemic
Patient
per day
performed
productivity
random intercept
recorded
reduction in
remote monitoring
Research
research coordinator
Satisfaction
significantly more
site initiation
site monitoring
solid tumor
Sponsor
statistically significant
study period
table
the median
the SARS-CoV-2
Total
translate
Trial
were excluded
[DOI] 10.1182/blood-2020-139937 [Article Type] Conference abstract
[DOI] 10.1182/blood-2020-139937 [Article Type] Conference abstract
Management of Renin-Angiotensin-Aldosterone System blockade in patients admitted to hospital with confirmed coronavirus disease (COVID-19) infection (The McGill RAAS-COVID- 19): A structured summary of a study protocol for a randomized controlled trial
코로나바이러스 감염증(COVID-19) 감염이 확인된 병원에 입원한 환자의 레닌-안지오텐신-알도스테론 시스템 차단 관리(The McGill RAAS-COVID-19): 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Study Protocol
[키워드] 1:1
48 hour
48 hours
ACE inhibitor
ACE2
Acute kidney injury
Admission
age
aldosterone
All participants
Amendment
Analysis
Anticoagulants
approach
assigned
baseline
Biomarker
Biomarkers
blinded
Blinding
blockade
blood pressure
BNP
C-reactive protein
C-reactive protein (CRP
calculated
calibrated
cardiovascular disease
change
Clinical improvement
clinical trials
collected
comparator
component
Consent
coronavirus disease
COVID-19
COVID-19 diagnosis
COVID-19 infection
COVID-19 patient
creatinine
creatinine)
CRP
database
death
diagnosis of COVID-19
died
discharge
dissemination
domains
doubling
Effect
EGFR
Ejection fraction
element
eligible
Endpoint
enrolment
Estimated
Ethnicity
evaluate
event
exclusion criteria
feasibility
Follow-up
followed by
General Hospital
greater
groups
Health
Health Organization
heart failure
high blood pressure
highest
hospital
ICU
ICU admission
immunopathology
include
Inclusion
inclusion and exclusion criteria
increase
increase in
Increases
indicate
Infection
inhibitor
inhibitors
initial
initiated
intervention arm
intravenous
invasive ventilation
list
Lower
lowest
lymphocyte
Lymphocyte count
lymphocyte counts
mathematical
mathematical model
McGill University
mean rank
mechanical ventilation
medical history
medication
medications
meet
Montreal
Mortality
number
objective
Older
open
open label
Ordinal Scale
outcome
outcomes
participant
Participants
past medical history
Patient
patient cohort
PCR
performed
Prevent
primary end point
primary endpoint
Protein
protocol
provided
RAAS
RAAS inhibitor
random number generator
randomised
randomised controlled trial
randomization
Randomized
Randomized controlled trial
recruitment
reduced
Registration
Renin
required
Sample
Sample size
SARS- CoV2
secondary
secondary endpoint
sensitivity
sensitivity analysis
serum creatinine
Sex
short term
stability
statistical power calculations
status
stroke
study participant
Study protocol
subsequent
supplementary material
System
table
team
the patient
the primary endpoint
therapy
transfer
transferred
Treatment
Trial
troponin
Version
Victoria
ward
website
were excluded
WHO
withdrawn
World Health Organization
[DOI] 10.1186/s13063-021-05080-4 PMC 바로가기 [Article Type] Study Protocol
[DOI] 10.1186/s13063-021-05080-4 PMC 바로가기 [Article Type] Study Protocol
Creation and maintenance of a table for assessment of evolving evidence for COVID-19-related treatments
COVID-19 관련 치료에 대한 진화하는 증거 평가를 위한 테이블 생성 및 유지
Review
[키워드] applied
available data
clinical trial
clinical trials
Comment
coronavirus disease
Coronavirus disease 2019
COVID-19
COVID-19 drug treatment
COVID-19 pandemic
creation
develop
dosage
drug
drug information
drug treatment
Efficacy
evaluate
Evidence
evidence-based practice
for inclusion
Healthcare professional
healthcare professionals
information
limitation
list
maintenance
pandemic
Pandemics
Patient
patients with COVID-19
point of care
Potential
Potential treatment
potential treatments
rationale
recommendation
regimens
resource
Society
supportive care
table
therapy
Treatment
Trial
[DOI] 10.1093/ajhp/zxaa334 PMC 바로가기 [Article Type] Review
[DOI] 10.1093/ajhp/zxaa334 PMC 바로가기 [Article Type] Review
The efficacy and safety of Ivermectin in patients with mild and moderate COVID-19: A structured summary of a study protocol for a randomized controlled trial
경증 및 중등도 COVID-19 환자에서 이버멕틴의 효능 및 안전성: 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Letter
[키워드] 1:1
ACE inhibitor
ACE inhibitors
acute respiratory syndrome
Adverse drug reaction
Adverse drug reactions
AIDS
allergy
anticipated
Anticoagulant
Anticoagulants
Asthma
Bandar Abbas
Blinding
Breastfeeding
Captopril
chest X-ray
clinical
clinical symptom
Clinical symptoms
clinical trial
clinical trials
company
Computed tomography
Confirmed
Control
control group
control groups
Controlled trial
COVID-19
COVID-19 symptom
criteria
Critical
CXR
Department
discharge
Diseases
dissemination
dose
Drug allergy
education
Efficacy and safety
element
evaluate
exclusion criteria
FIVE
France
group
groups
history
Hospital stay
Hospitalization
Hospitalization Mechanical ventilation
hydroxychloroquine sulfate
ICU admission
incidence
include
inclusion criteria
India
Infection
Informed consent
Inpatients
Interferon beta-1a
intervention group
Iran
Ivermectin
Kidney disease
liver
loiasis
Lopinavir
Lopinavir/ritonavir
mechanical ventilation
Mild
mild COVID-19 symptom
mild COVID-19 symptoms
mild pneumonia
Ministry of Health
moderate
Moderate COVID-19
moderately severe COVID-19
MSD
number
objective
Open-label
Other
outcome
Outpatient
outpatients
parallel-group
participant
Patient
patients
patients with moderate
PCR
pharmaceutical
Pharmaceutical Company
Phase 3
Pneumonia
Pregnancy
Primary outcome
Primary outcomes
protocol
random
randomization
Randomized
Randomized controlled trial
receive
regimen
Registered
registration date
registration number
registry
respiratory
Ritonavir
routine care
Sample size
secondary outcome
selected
Seven
Severe acute respiratory syndrome
single dose
single-center
standard treatment
status
Study protocol
subsequent
supplementary material
table
the patient
Treatment
treatment group
Trial registration
twice a day
two group
two groups
underlying diseases
Version
Warfarin
website
weight
[DOI] 10.1186/s13063-020-04988-7 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04988-7 PMC 바로가기 [Article Type] Letter
Psychiatric Adverse Drug Reactions and Potential Anti-COVID-19 Drug Interactions with Psychotropic Medications
Review Article
[키워드] ADRS
Adverse
Adverse drug reaction
Adverse drug reactions
Complication
Coronavirus disease 2019
COVID-19
disease severity
drug
drug-drug interaction
Drug-drug interactions
induce
involved
literature review
management
Patient
patients
pharmacokinetics
Potential
potential mechanism
provided
Psychiatric
psychiatric disorder
psychiatry
psychological Impact
Psychotropic
Psychotropic medication
reaction
table
Treatment
[DOI] 10.22037/ijpr.2021.114717.15007 PMC 바로가기 [Article Type] Review Article
[DOI] 10.22037/ijpr.2021.114717.15007 PMC 바로가기 [Article Type] Review Article
Ivermectin to prevent hospitalizations in patients with COVID-19 (IVERCOR-COVID19): a structured summary of a study protocol for a randomized controlled trial
COVID-19(IVERCOR-COVID19) 환자의 입원을 방지하기 위한 Ivermectin: 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Randomized Controlled Trial
[키워드] 1:1
acute infectious disease
addition
adherence
administration
Admission
adverse event
adverse events
age
allergy
analyzed
Anthropometric data
antiviral drug
antiviral drugs
Arm
ARMS
assessment
barrier
basal
blinded
Breastfeeding
breastfeeding women
Cardiology
Care
care providers
carried
cause
Chain Reaction
childbearing age
Chloroquine
cirrhosis
component
components
Concomitant
Concomitant medication
Confirmed
connection
contraceptive method
contraceptives
Control
control group
control groups
coordination
Corriente
COVID-19
COVID-19 patient population
criteria
current
Day
death
demographic
demographic data
Diagnosis
diagnosis of COVID-19
dialysis
discharged
dissemination
dose
double-blind
drug
Efficacy
Efficacy and safety
elapsed
element
EOS
Equal
example
exclusion criteria
Final
final visit
first dose
Follow-up
greater
heart rate
Hospitalization
hospitalizations
Hydroxychloroquine
incidence
include
Inclusion
inclusion criteria
inclusion/exclusion criteria
Informed consent
Intervention
Invasive mechanical ventilation
investigator
investigators
Ivermectin
Ivermectin safety
Laboratory
less
liver
Liver cirrhosis
Liver disease
mal-absorptive syndrome
medical history
medication
menstrual
menstrual cycles
Mortality
negative
Negative PCR
number
objective
outcome
outcome assessor
outcome assessors
over
oxygen
oxygen saturation
parallel group
participant
Participants
Participation
Patient
patients with COVID-19
PCR
PCR swab
Placebo
placebo-controlled study
polymerase chain
polymerase chain reaction
Polymerase chain reaction test
postmenopausal
pregnant
Presence
Prevent
Primary outcome
protocol
Public
public health
randomization
Randomized
Randomized controlled trial
randomly permuted blocks
receive
recommendation
recorded
recruitment
reducing
renal replacement therapy
replacement therapy
reproductive
required
Research
Sample size
SARS-CoV2
secondary
severe liver disease
single-center
standard treatment
standard treatment alone
Study protocol
supplementary material
surgical
Swab
table
Tablet
temperature
the patient
Total
Treatment
Trial
Trial registration
use of hydroxychloroquine
Version
Viral
viral pathology
Vital
vital signs
vital status
web system
website
weight
woman
women
[DOI] 10.1186/s13063-020-04813-1 PMC 바로가기 [Article Type] Randomized Controlled Trial
[DOI] 10.1186/s13063-020-04813-1 PMC 바로가기 [Article Type] Randomized Controlled Trial
A Risk Prediction Model for Evaluating the Disease Progression of COVID-19 Pneumonia
Medicine
[키워드] acute respiratory syndrome
age
Algorithm
Analysis
caused
China
Cohort
cohorts
Comorbidities
coronavirus
coronavirus disease
COVID 19
COVID-19
CREA
diabetes
Disease progression
enrolled
Epidemic
evaluate
Evaluating
Factor
Fever
help
hospital
hypertension
identify
Infection
Laboratory
LDH
Logistic
Logistic regression
men
Meta-analysis
Model
neutrophil count
Patient
Pneumonia
prediction
progression
risk
risk factor
Risk prediction model
SARS-CoV2
Severe COVID-19 pneumonia
shown
significantly
sSARS—CoV-2
table
the disease
the median
validation cohort
validation cohorts
was performed
with COVID-19
women
Wuhan
[DOI] 10.3389/fmed.2020.556886 PMC 바로가기 [Article Type] Medicine
[DOI] 10.3389/fmed.2020.556886 PMC 바로가기 [Article Type] Medicine
COVID-19 in Patients with Hematologic Malignancies: A Single-Center Experience
Conference abstract
[키워드] Absolute lymphocyte count
active cancer
acute respiratory syndrome
age
ALC
Allogeneic
autologous
B-cell lymphoma
board
Cancer therapy
cardiac disease
Care
Cell
center
Cohort
cohort of patient
collected
Comorbidities
Complication
conditions
conducted
coronavirus
cough
COVID-19
COVID-19 diagnosis
COVID-19 in patient
COVID-19 infection
database
defined
demographic characteristics
described
Diagnosis
diagnosis of COVID-19
died
download
electronic medical records
expected
experience
Fever
for inclusion
funding
health system
Hematologic malignancy
higher risk
HM patient
Hospital admission
ICU
immune dysfunction
impacted
include
Infection
Innate
intubation
Jazz
Kiowa
laboratory data
lymphopenia
majority
median
mortality rate
Multiple myeloma
Nasopharyngeal swab
network
Older age
outcome
pandemic
Patient
patients
patients with HM
positive result
presenting symptom
presenting symptoms
Prevalence
promote
rates of infection
real-time RT-PCR
required
Retrospective study
risk factor
robust
SARS-CoV-2
SCT
Seattle
severe COVID-19
Shortness of breath
shown
Smokers
social distancing
specimen
subsequent
supportive care
symptomatic
table
therapy
treated
Treatment
Two patient
underlying disease
with COVID-19
[DOI] 10.1182/blood-2020-140719 [Article Type] Conference abstract
[DOI] 10.1182/blood-2020-140719 [Article Type] Conference abstract
Biomarkers of Hypercoagulability and Endothelial Cell Activation in Patients with Severe COVID-19 Admitted at the Intensive Care Unit. the Roadmap-COVID-19 Prospective Observational Study
Conference abstract
[키워드] Activation
acute respiratory distress
acute respiratory syndrome
Algorithm
Antithrombotic
AP-HP
ARDS
Biomarker
Blood coagulation
calculated
cause
cellular
change
characterized
clinically
clotting factor
Cluster
Coagulation
cohort study
complications
consecutive patient
Control
control group
controls
coronavirus
coronavirus disease
COVID-19
D-dimer
decrease
disease
download
effect of treatment
endothelial
Endothelial cell
Endothelial dysfunction
enrolled
evaluate
evaluated
excessive inflammation
expressing
fibrinogen
FVIII
healthy individual
Heparanase
Hospitalized
hypercoagulability
ICU
ICU admission
ICU patient
IL-6
IL-6 level
increase
indicate
indicated
inflammatory reaction
Inhaled
inhibitor
intensive care unit
intrinsic
life-threatening
LMWH
management
mandatory
Microparticle
moderate
modify
molecular weight
monomer
MRI
Multisystem organ failure
outcome
Paris
pathway
Patient
patients
patients hospitalized
patients with COVID-19
peak
platelet activation
Pneumonia
Prospective
Prospective Study
Protein
protein S
ranged
Ratio
Respiratory failure
Result
SARS-CoV-2
SARS-COV-2 infection
severe COVID-19
shown
significant decrease
significantly
STABLE
syndrome
table
TFPI
the mean
the patient
thrombin
Thromboprophylaxis
university
von Willebrand factor
were assessed
with COVID-19
[DOI] 10.1182/blood-2020-140275 [Article Type] Conference abstract
[DOI] 10.1182/blood-2020-140275 [Article Type] Conference abstract