Systematic review of registered trials of Hydroxychloroquine prophylaxis for COVID-19 health-care workers at the first third of 2020.

One Health

Univ Lyon, Malaria Research Unit, ICBMS, UMR 5246 CNRS INSA CPE, F-69100, Lyon, France.

Published: December 2020

AI Article Synopsis

  • The medical community is exploring the use of pre or post-exposure drugs, like Hydroxychloroquine (HCQ), to minimize the risk and severity of COVID-19, especially in the absence of a vaccine.
  • A systematic review of interventional studies found that most studies on HCQ were well-designed, with a variety of dosing regimens currently being investigated globally.
  • It’s essential to conduct thorough evaluations of these studies’ clinical designs to understand the results accurately, instead of relying on simplified social media summaries that may misrepresent the findings.

Article Abstract

In the absence of a vaccine the medical and scientific community is looking intensely at utilizing a pre or post exposure drug that could decrease viremia. The search for a medication that could reduce risk of serious disease, and ideally of any manifestation of disease from SARS-CoV2, and of asymptomatic shedding of SARS-CoV2 is of urgent interest. Repurposing existing pharmaceuticals is among the approaches to achieve these ends. We performed a systematic review of all interventional studies registered in ClinicalTrials.gov with a focus on one repurposed drug, Hydroxychloroquine (HCQ). The detailed analysis of these studies, some of them already recruiting, provide an overall picture of HCQ use as a COVID-19 prophylaxis around the world. Among the included studies, all but three were randomized and parallel and most of them (74%, 23/31) were double-blinded to quadruple-blinded studies. We found a great diversity in dosing and nearly all the possible scientifically reasonable regimens are under evaluation. This diversity offers benefits as well as challenges. Importantly, the final analysis of these trials should be done through an extensive reading of the results in regard to the clinical design, it will be crucial to carefully read and evaluate the results of each study in regards to the clinical design rather than quickly glancing a 140 characters-based social media message announcing the failure or success of a drug against a disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235596PMC
http://dx.doi.org/10.1016/j.onehlt.2020.100141DOI Listing

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