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Efficacy and safety of nitazoxanide in treating SARS-CoV-2 infection: a systematic review and meta-analysis of blinded, placebo-controlled, randomized clinical trials.
Martins-Filho, Paulo Ricardo; do Nascimento-Júnior, Edmundo Marques; Barreto-Alves, José Antônio; Fakhouri, Ricardo; Ferreira, Lis Campos.
  • Martins-Filho PR; Investigative Pathology Laboratory, Federal University of Sergipe, Rua Cláudio Batista, s/n. Bairro Sanatório, Aracaju, Sergipe, 49060-100, Brazil. prmartinsfh@gmail.com.
  • do Nascimento-Júnior EM; Health Sciences Graduate Program, Federal University of Sergipe, Aracaju, Sergipe, Brazil. prmartinsfh@gmail.com.
  • Barreto-Alves JA; Investigative Pathology Laboratory, Federal University of Sergipe, Rua Cláudio Batista, s/n. Bairro Sanatório, Aracaju, Sergipe, 49060-100, Brazil.
  • Fakhouri R; Department of Nursing, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
  • Ferreira LC; Department of Medicine, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
Eur J Clin Pharmacol ; 78(11): 1813-1821, 2022 Nov.
Article in English | MEDLINE | ID: covidwho-2007128
ABSTRACT

PURPOSE:

Nitazoxanide is a broad-spectrum antiparasitic that has been tested for COVID-19 due to its anti-inflammatory effects and in vitro antiviral activity. This study synthesized the best evidence on the efficacy and safety of nitazoxanide in COVID-19.

METHODS:

Searches for studies were performed in peer-reviewed and grey-literature from January 1, 2020 to May 23, 2022. The following elements were used to define eligibility criteria (1) Population individuals with COVID-19; (2) Intervention nitazoxanide; (3) Comparison placebo; (4)

Outcomes:

primary outcome was death, and secondary outcomes were viral load, positive RT-PCR status, serum biomarkers of inflammation, composite measure of disease progression (ICU admission or invasive mechanical ventilation), and any adverse events; (5) Study type blinded, placebo-controlled, randomized clinical trials (RCTs). Treatment effects were reported as relative risk (RR) for dichotomous variables and standardized mean difference (SMD) for continuous variables with 95% confidence intervals (CI).

RESULTS:

Five blinded, placebo-controlled RCTs were included and enrolled individuals with mild or moderate SARS-CoV-2 infection. We found no difference between nitazoxanide and placebo in reducing viral load (SMD = - 0.16; 95% CI - 0.38 to 0.05) and the frequency of positive RTP-PCR results (RR = 0.92; 95% CI 0.81 to 1.06). In addition, there was no decreased risk for disease progression (RR = 0.63; 95% CI 0.38 to 1.04) and death (RR = 0.81; 95% CI 0.36 to 1.78) among patients receiving nitazoxanide. Patients with COVID-19 treated with nitazoxanide had decreased levels of white blood cells (SMD = - 0.15; 95% - 0.29 to - 0.02), lactate dehydrogenase (LDH) (SMD - 0.32; 95% - 0.52 to - 0.13), and D-dimer (SMD - 0.49; 95% CI - 0.68 to - 0.31) compared to placebo, but the magnitude of effect was considered small to moderate.

CONCLUSION:

This systematic review showed no evidence of clinical benefits of the use of nitazoxanide to treat patients with mild or moderate COVID-19. In addition, we found a reduction in WBC, LDH, and D-dimer levels among nitazoxanide-treated patients, but the effect size was considered small to moderate.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Limits: Humans Language: English Journal: Eur J Clin Pharmacol Year: 2022 Document Type: Article Affiliation country: S00228-022-03380-5

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Limits: Humans Language: English Journal: Eur J Clin Pharmacol Year: 2022 Document Type: Article Affiliation country: S00228-022-03380-5