Rationale and Design of the COVID-19 Outpatient Prevention Evaluation (COPE - Coalition V) Randomized Clinical Trial: Hydroxychloroquine vs. Placebo in Non-Hospitalized Patients

被引:0
|
作者
de Oliveira Junior, Haliton Alves [1 ]
Ferri, Cleusa P. [1 ]
Boszczowski, Icaro [1 ]
Oliveira, Gustavo B. F. [1 ]
Cavalcanti, Alexandre B. [2 ,3 ]
Rosa, Regis G. [3 ,4 ]
Lopes, Renato D. [5 ,6 ]
Azevedo, Luciano C. P. [3 ,7 ]
Veiga, Viviane C. [3 ,8 ]
Berwanger, Otavio [9 ]
Avezum, Alvaro [1 ]
机构
[1] Hosp Alemao Oswaldo Cruz, Ctr Int Pesquisa, Sao Paulo, SP, Brazil
[2] Inst Pesquisa HCor, Sao Paulo, SP, Brazil
[3] Brazilian Res Intens Care Network BRICnet, Sao Paulo, SP, Brazil
[4] Hosp Moinhos Vento, Porto Alegre, RS, Brazil
[5] Brazilian Clin Res Inst BCRI, Sao Paulo, SP, Brazil
[6] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC USA
[7] Hosp Sirio Libanes, Inst Ensino & Pesquisa, Sao Paulo, SP, Brazil
[8] Beneficencia Portuguesa Sao Paulo, Sao Paulo, SP, Brazil
[9] Hosp Israelita Albert Einstein, Acad Res Org, Sao Paulo, SP, Brazil
关键词
COVID-19; SARS-CoV-2; Hydroxychloroquine; Randomized Controlled Trial;
D O I
10.36660/abc.20210832
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Despite the need for targeting specific therapeutic options for coronavirus disease 2019 (COVID-19), there has been no evidence of effectiveness of any specific treatment for the outpatient clinical setting. There are few randomized studies evaluating hydroxychloroquine (HCQ) in non-hospitalized patients. These studies indicate no benefit from the use of HCQ, but they assessed different primary outcomes and presented important biases for outcome evaluation. Objective: To evaluate if HCQ may prevent hospitalization due to COVID-19 compared to a matching placebo. Methods: The COVID-19 Outpatient Prevention Evaluation (COPE) study is a pragmatic, randomized, double-blind, placebo-controlled clinical trial evaluating the use of HCQ (800 mg on day 1 and 400 mg from day 2 to day 7) or matching placebo for the prevention of hospitalization due to COVID-19 in early non-hospitalized confirmed or suspected cases. Inclusion criteria are adults (>= 18 years) seeking medical care with mild symptoms of COVID-19, with randomization <= 7 days after symptom onset, without indication of hospitalization at study screening, and with at least one risk factor for complication (> 65 years; hypertension; diabetes mellitus; asthma; chronic obstructive pulmonary disease or other chronic lung diseases; smoking; immunosuppression; or obesity). All hypothesis tests will be two-sided. A p-value < 0.05 will be considered statistically significant in all analyses. Clinicaltrials.gov: NCT04466540. Results: Clinical outcomes will be centrally adjudicated by an independent clinical event committee blinded to the assigned treatment groups. The primary efficacy endpoint will be assessed following the intention-to-treat principle. Conclusion: This study has the potential to reliably answer the scientific question of HCQ use in outpatients with COVID-19. To our knowledge, this is the largest trial evaluating HCQ in non-hospitalized individuals with COVID-19.
引用
收藏
页码:378 / 386
页数:9
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