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Trial to Evaluate Efficacy and Safety of Nitazoxanide in the Treatment of Colds Due to Enterovirus/Rhinovirus Infection

NCT04489381 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 214

Last updated 2024-10-17

Study results available
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Summary

Trial to evaluate the efficacy and safety of nitazoxanide in the treatment of colds due to enterovirus/rhinovirus infection

Conditions

  • Enterovirus
  • Rhinovirus

Interventions

DRUG

Nitazoxanide

Two nitazoxanide 300 mg tablets administered orally twice daily with food for 5 days

DRUG

Placebo

Two placebo tablets administered orally twice daily with food for 5 days

DIETARY_SUPPLEMENT

Vitamin Super B-Complex

Vitamin Super B-Complex administered orally twice daily to maintain the blind

Sponsors & Collaborators

  • Romark Laboratories L.C.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-19
Primary Completion
2021-01-28
Completion
2021-02-02
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04489381 on ClinicalTrials.gov