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Terminated Phase 2 Interventional

Study of Nitazoxanide Tablets in the Treatment of Mild to Moderate Active Crohn's Disease

ClinicalTrials.gov ID: NCT00130390

Public ClinicalTrials.gov record NCT00130390. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 8:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multi-center, Randomized, Double-Blind, Placebo-Controlled Trial of Nitazoxanide Tablets in the Treatment of Mild to Moderate Active Crohn's Disease in Adults

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to evaluate the efficacy and safety of nitazoxanide compared to a placebo in reducing the signs and symptoms of mild to moderate active Crohn's disease in adults.

Study identification

NCT ID
NCT00130390
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Romark Laboratories L.C.
Industry
Enrollment
98 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2005
Primary completion
Nov 30, 2007
Completion
Jun 30, 2008
Last update posted
May 30, 2012

2005 – 2008

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
13
Facility City State ZIP Site status
Romark Laboratories, L.C. Tampa Florida 33607
Florida medical Clinic, P.A. Zephyrhills Florida 33542
Atlanta Gastroenterology Marietta Georgia 30067
Atlanta Gastroenterology Woodstock Georgia 30189
Gasteroenterology Associates Baton Rouge Louisiana 70809
Minnesota Gastroenterology, P.A., Clinical Research Division Plymouth Minnesota 55446
Long Island Clinical Research Associates, LLP Great Neck New York 11021
Greater Cincinnati Gastroenterology Associates Cincinnati Ohio 45219
Digestive Research & Infusion Institute Mayfield Heights Ohio 44124
Oklahoma Foundation for Digestive Research Oklahoma City Oklahoma 73104
Memphis Gastroenterology Group Germantown Tennessee 38138
Gastrointestinal Associates, LLC Kingsport Tennessee 37660
Nashville Medical Research Nashville Tennessee 37205

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00130390, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 30, 2012 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00130390 live on ClinicalTrials.gov.

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