Hydroxychloroquine in the treatment of adult patients with Covid-19 infection in a primary care setting (LIBERTY): A structured summary of a study protocol for a randomised controlled trial
일차 진료 환경(LIBERTY)에서 Covid-19 감염 성인 환자 치료에 사용되는 하이드록시클로로퀸: 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Letter
[키워드] 1:1
addition
addressed
administration
Adult patients
adverse event
adverse events
AEs
age
all-cause hospitalization
Antibody Response
Anxiety
Anxiety Disorder
ARMS
association
Biomarker
blinded
Blinding
Blood
BMI
capture
Care
changes
changes in
Characteristics
clinical trial
concentrations
concomitant medications
conducted
Contact
Course
COVID-19
COVID-19 infection
COVID-19-related symptoms
criteria
death
deleting
Demographic variables
diabetes
Diabetes Mellitus
disease
dissemination
double-blind
Effect
element
enrolment
enzyme
EudraCT
evaluate
exclusion
expected
exploratory
exploratory endpoint
Exploratory endpoints
female
Formulation
GAD-7
Generalized
Generalized Anxiety Disorder
Genetic variation
HCQ
Health care
HLA haplotypes
hospital
Hospitalization
hospitalizations
Hydroxychloroquine
Hypothesis
identify
include
Inclusion
independent
individual
Infection
information
intensive care unit
lactation
masking
mental health
Meta-analysis
Mortality
Nasopharyngeal swab
nasopharyngeal swab sample
Nasopharyngeal swab samples
number
number of deaths
objective
onset of symptom
open care
outcome
Outpatient
outpatients
parallel-group
participant
Patient
patient data
PCR test
PCR testing
PCR-confirmed
Placebo
placebo-controlled
post-hoc
predict
Pregnancy
presenting
primary care
primary endpoint
protocol
public health
public health care
randomised
randomised controlled trial
randomization list
Randomized
Randomly
receive
recruitment
reduce
Registered
Regulation
repeated
reported
respiratory
respiratory distress
respiratory rate
response
risk
room air
SAEs
Sample size
SARS-CoV-2
SARS-CoV-2 PCR test
SARS-CoV-2 viral shedding
Satakunta
secondary endpoint
Secondary endpoints
Secondary objectives
serious AE
serum
Seven
severe pneumonia
severity
specific treatment
status
study participant
Study participants
study population
Study protocol
subgroup analysis
subject
supplementary material
Suspected
Symptom
Symptoms
technology
test result
therapeutic potential
Tolerability
treated
Treatment
treatment allocation
treatment arm
Trial
Trial registration
twice a day
type 1 or type 2
Uppsala
variable
Viral
was performed
website
Well-being
[DOI] 10.1186/s13063-020-04989-6 PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-020-04989-6 PMC 바로가기 [Article Type] Letter