Efficacy of chloroquine versus lopinavir/ritonavir in mild/general COVID-19 infection: a prospective, open-label, multicenter, randomized controlled clinical study

被引:14
|
作者
Liu, Xi [1 ]
Chen, Huili [1 ]
Shang, Yuqi [1 ]
Zhu, Hongqiong [1 ]
Chen, Gongqi [1 ]
Chen, Yuanli [2 ]
Liu, Shaoxuan [3 ]
Zhou, Yaoyong [1 ]
Huang, Mingxing [1 ]
Hong, Zhongsi [1 ]
Xia, Jinyu [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Infect Dis, Zhuhai, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Hosp Infect Control, Zhuhai, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 5, Off Clin Res Ctr, Zhuhai, Peoples R China
关键词
COVID-19; Chloroquine; Lopinavir; ritonavir; Randomized controlled clinical study; Efficacy; CORONAVIRUS; INHIBITION; ENTRY; DRUG;
D O I
10.1186/s13063-020-04478-w
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundThe outbreak of COVID-19 (caused by SARS-Cov-2) is very serious, and no effective antiviral treatment has yet been confirmed. The adage "old drug, new trick" in this context may suggest the important therapeutic potential of existing drugs. We found that the lopinavir/ritonavir treatment recommended in the fifth edition of the Treatment Plan of China can only help to improve a minority of throat-swab nucleic-acid results (3/15) in hospitals. Our previous use of chloroquine to treat patients with COVID-19 infection showed an improvement in more throat-swab nucleic-acid results (5/10) than the use of lopinavir/ritonavir.Methods/designThis is a prospective, open-label, randomized controlled, multicenter clinical study. The study consists of three phases: a screening period, a treatment period of no more than 10days, and a follow-up period for each participant. Participants with COVID-19 infection who are eligible for selection for the study will be randomly allocated to the trial group or the control group. The control group will be given lopinavir/ritonavir treatment for no more than 10days. The trial group will be given chloroquine phosphate treatment for no more than 10days. The primary outcome is the clinical recovery time at no more than 28days after the completion of therapy and follow-up. The secondary outcomes include the rate of treatment success after the completion of therapy and follow-up, the time of treatment success after no more than 28days, the rate of serious adverse events during the completion of therapy and follow-up, and the time to return to normal temperature (calculated from the onset of illness) during the completion of therapy and follow-up. Comparisons will be performed using two-sided tests with a statistical significance level of 5%.DiscussionThis experiment should reveal the efficacy and safety of using chloroquine versus lopinavir/ritonavir for patients with mild/general COVID-19 infection. If the new treatment including chloroquine shows a higher rate of throat-swab SARS-CoV-2 real-time fluorescent reverse transcription polymerase chain reaction (RT-PCR) negativity and is safe, it could be tested as a future COVID-19 treatment.Trial registrationChinese Clinical Trial Registry, ID: ChiCTR2000029741. Registered on 11 February 2020.
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页数:9
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