Nitazoxanide/azithromycin combination for COVID-19: A suggested new protocol for early management.
Mina T Kelleni
https://pubmed.ncbi.nlm.nih.gov/32360581Actively Recruiting
Led by Tanta University · Updated on 2020-12-04
160
Participants Needed
2
Research Sites
N/A
Total Duration
Researchers are evaluating the use of Nitazoxanide for treating COVID-19, a viral infection caused by the severe acute respiratory syndrome coronavirus 2. This study aims to assess the clinical effectiveness of Nitazoxanide compared to the standard treatment protocol. The trial is conducted by Tanta University and is a Phase 3 randomized study without masking. Participants are assigned to one of two groups: one receiving Nitazoxanide alongside the standard treatment, and the other receiving only the standard treatment. The study explores the potential benefits of Nitazoxanide, which has shown clinical efficacy, alongside other drugs like ivermectin and azithromycin in previous research. During the study, researchers monitor patients over six months, focusing on the number of patients achieving virological cure. Participants will undergo regular assessments to track their response to treatment. The study does not include blinding, and no placebo is used. Safety and efficacy are evaluated throughout the trial period, which began in May 2020 and is expected to end by December 2030.
CONDITIONS
Novel Regimens in COVID-19 Treatment
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Participants receive Nitazoxanide or standard treatment for COVID-19 as part of the study.
Total: 2 locations
1
Tanta University, Assiut University
Tanta, Egypt, 35111
Actively Recruiting
2
Sherief Abd-Elsalam
Tanta, Egypt
Actively Recruiting
S
Sherief Abd-Elsalam, ass. prof.
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Mina T Kelleni
https://pubmed.ncbi.nlm.nih.gov/32360581R Choudhary, A K Sharma
https://pubmed.ncbi.nlm.nih.gov/32322397