Actively Recruiting

Phase 3
Age: 18Years +
All Genders
ID04382846

Nitazoxanide in Treatment of COVID-19

Led by Tanta University · Updated on 2020-12-04

160

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Novel Regimens in COVID-19 Treatment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with COVID-19 infection
Not Eligible

You will not qualify if you...

  • Allergy or contraindication to the drugs.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Participants receive Nitazoxanide or standard treatment for COVID-19 as part of the study.

Trial Site Locations

Total: 2 locations

1

Tanta University, Assiut University

Tanta, Egypt, 35111

Actively Recruiting

2

Sherief Abd-Elsalam

Tanta, Egypt

Actively Recruiting

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Research Team

S

Sherief Abd-Elsalam, ass. prof.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial