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Published in: BMC Infectious Diseases 1/2022

Open Access 01-12-2022 | SARS-CoV-2 | Research

Ivermectin compared with placebo in the clinical course in Mexican patients with asymptomatic and mild COVID-19: a randomized clinical trial

Authors: Carmen de la Rocha, Marco A. Cid-López, Blanca I. Venegas-López, Sandra C. Gómez-Méndez, Adriana Sánchez-Ortiz, Alma M. Pérez-Ríos, Ricardo A. Llamas-Velázquez, Aidé I. Meza-Acuña, Bárbara Vargas-Íñiguez, Daniela Rosales-Galván, Alejandra Tavares-Váldez, Nizdali Luna-Gudiño, Cinthia V. Hernández-Puente, Jovana Milenkovic, Cecilia Iglesias-Palomares, Miriam Méndez-del Villar, Gerardo A. Gutiérrez-Dieck, Carlos G. Valderrábano-Roldán, Jennefer Mercado-Cerda, Jocelyn G. Robles-Bojórquez, Arieh R. Mercado-Sesma

Published in: BMC Infectious Diseases | Issue 1/2022

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Abstract

Background

Despite the development and application of vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) around the world, the scientific community is still trying to find some therapies to avoid or ameliorate the fatal evolution of the Coronavirus disease 2019 (COVID-19). Since the publication of the potential use of ivermectin as a treatment against the disease, a pleiad of information about it has been published. However, the evidence is not strong or weak enough to conclude its usefulness in the clinical evolution of patients infected with SARS-CoV-2. We evaluate the efficacy and safety of ivermectin in the treatment of Mexican patients with asymptomatic and mild COVID-19 in a three-day administration in comparison to placebo.

Methods

A randomized, double-blind, placebo-controlled trial was carried out in 66 adults with asymptomatic and mild COVID-19. Patients were randomly assigned 1:1 ratio to ivermectin plus acetaminophen or placebo plus acetaminophen. The primary endpoint was the proportion of subjects without a disease progression to severity according to COVID-19 guidelines by the National Institutes of Health (NIH) since randomization to 14 days.

Results

None of the participants presented progression to a severe state in either group. Viral load was measured on Days 1, 5, and 14. No significant differences were observed in baseline or 14-day between groups (p = 0.720 and 0.362, respectively). However, on Day 5, a significant difference in viral load was observed between groups (p = 0.039). The frequency of symptoms was similar between groups, and no significant differences were observed. The most frequent symptom was cough. One severe adverse event associated with SARS-CoV-2 infection was observed in the ivermectin group.

Conclusions

At standard doses, ivermectin is not effective to prevent progression to a severe state or reducing symptoms in adults with asymptomatic and mild COVID-19.
Trial registration The study was registered with ClinicalTrial.gov (NCT04407507) on May 29, 2020.
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Metadata
Title
Ivermectin compared with placebo in the clinical course in Mexican patients with asymptomatic and mild COVID-19: a randomized clinical trial
Authors
Carmen de la Rocha
Marco A. Cid-López
Blanca I. Venegas-López
Sandra C. Gómez-Méndez
Adriana Sánchez-Ortiz
Alma M. Pérez-Ríos
Ricardo A. Llamas-Velázquez
Aidé I. Meza-Acuña
Bárbara Vargas-Íñiguez
Daniela Rosales-Galván
Alejandra Tavares-Váldez
Nizdali Luna-Gudiño
Cinthia V. Hernández-Puente
Jovana Milenkovic
Cecilia Iglesias-Palomares
Miriam Méndez-del Villar
Gerardo A. Gutiérrez-Dieck
Carlos G. Valderrábano-Roldán
Jennefer Mercado-Cerda
Jocelyn G. Robles-Bojórquez
Arieh R. Mercado-Sesma
Publication date
01-12-2022
Publisher
BioMed Central
Published in
BMC Infectious Diseases / Issue 1/2022
Electronic ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-022-07890-6

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