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DOI 10.36660/abc.20210832

Медицинская библиотека · Arquivos brasileiros de cardiologia · 2022

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

Oliveira Junior Haliton Alves de, Ferri Cleusa P, Boszczowski Icaro, Oliveira Gustavo B F, Cavalcanti Alexandre B, Rosa Regis G, Lopes Renato D, Azevedo Luciano C P, Veiga Viviane C, Berwanger Otavio, Avezum Álvaro

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Аннотация

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.

Для цитирования: Oliveira Junior Haliton Alves de, Ferri Cleusa P, Boszczowski Icaro, Oliveira Gustavo B F, Cavalcanti Alexandre B, Rosa Regis G, Lopes Renato D, Azevedo Luciano C P, Veiga Viviane C, Berwanger Otavio, Avezum Álvaro. Rationale and Design of the COVID-19 Outpatient Prevention Evaluation (COPE - Coalition V) Randomized Clinical Trial: Hydroxychloroquine vs. Placebo in Non-Hospitalized Patients.. Arquivos brasileiros de cardiologia. 2022. DOI: 10.36660/abc.20210832.

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