Efficacy and safety of nelfinavir in asymptomatic and mild COVID-19 patients: a structured summary of a study protocol for a multicenter, randomized controlled trial
무증상 및 경증 COVID-19 환자에 대한 nelfinavir의 효능 및 안전성: 다기관, 무작위 대조 시험을 위한 연구 프로토콜의 구조화된 요약
Letter
[키워드] 1:1
Administered
administration
adverse event
adverse events
age
all-cause mortality
ALT
Analysis
anticipated
Antigen
antiviral efficacy
AST
Asymptomatic
asymptomatic patients
blinded
blinded outcome assessment
Blinding
blood glucose
body temperature
both group
both groups
capture
caused
childbearing potential
clearance
clinical
Clinical efficacy
clinical examinations
Clinical symptoms
clinical trial
clinical trials
comparator Patients
condition
Consent
contraceptive method
Controlled clinical trial
cough
COVID-19
creatinine
creatinine clearance
dataset
Day
defervescence
diabete
diabetes
diarrhea
discretion
dissemination
distribution
drug
element
enrolled
enrolment
evaluate
event
exclusion criteria
exploratory
Factor
female patient
Fever
Frequency
Glucose
group
hazard ratio
Hemophiliac
Hemorrhagic
history
HIV infection
hospital
hypersensitivity
incidence
incidence rate
Inclusion
inclusion and exclusion criteria
inclusion criteria
Infection
Informed consent
initial
investigator
investigator-initiated
investigators
Japan
Japanese
LAMP
limit
log-rank test
male
Mild
mild COVID-19 patient
Mild disease
mixed-effects model
multicenter
Nasopharyngeal swab
Negative conversion
Negative PCR
nelfinavir
null hypothesis
number
objective
Open-label
outcome
oxygen
Oxygen administration
p value
parallel group
parameter
participant
Patient
patients with asymptomatic
PCR
PCR test
Pneumonia
power
Pregnancy
primary endpoint
Primary outcome
principal investigator
Probability
probability distribution
protocol
random
randomization
Randomized
Randomized controlled trial
Registered
registry
reported
required
respiratory tract
rifampicin
room air
safety endpoint
Saliva
saliva samples
Sample size
SARS-CoV-2
SARS-CoV-2 vaccination
secondary efficacy endpoint
serious complication
serum creatinine
severity
specimen
Standard
status
study period
Study protocol
supplementary material
survival
survival function
Symptom
symptomatic
symptomatic COVID-19
Symptomatic treatment
the log-rank test
Three times daily
Treatment
treatment for HIV
treatment period
Trial
Trial registration
two-sided
Unsuitable
Viral
viral dynamics
Viral load
virus
was determined
website
Withdrawal
withdrawal of consent
[DOI] 10.1186/s13063-021-05282-w PMC 바로가기 [Article Type] Letter
[DOI] 10.1186/s13063-021-05282-w PMC 바로가기 [Article Type] Letter