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NCT00130390 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Romark Laboratories L.C..

Terminated
Registry status
Phase 2
Development phase
98
Enrollment target

NCT00130390: Clinical Trial Phase 2 study, sponsored by Romark Laboratories L.C..

NCT00130390 is a Phase 2 study that was terminated before completion, run by Romark Laboratories L.C.. The registered enrollment target is 98 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (26% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00130390, a Phase 2 study, was terminated before completion, sponsored by Romark Laboratories L.C..

TERMINATED
Registry status
Phase 2
Development phase
98 participants
Enrollment target

Study Summary

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.

Interventions

  • OTHER Placebo
  • DRUG Nitazoxanide

Trial Details

FieldValue
Enrollment Target 98 participants
Start Date 2005-08
Est. Completion 2008-07
Phase Phase 2
Romark Laboratories L.C.

16 total trials

Why NCT00130390 stopped before completion

NCT00130390 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 98 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (26% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00130390 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00130390 about?

NCT00130390 is a clinical study titled "Study of Nitazoxanide Tablets in the Treatment of Mild to Moderate Active Crohn's Disease". 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.

What is the current status of trial NCT00130390?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 98 participants. The study started on 2005-08. Estimated completion is 2008-07.

What interventions are being tested in trial NCT00130390?

The interventions under investigation include: Placebo (OTHER), Nitazoxanide (DRUG).

Who is sponsoring clinical trial NCT00130390?

This trial is sponsored by Romark Laboratories L.C., which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00130390's enrollment target sits among peer trials

98 743rd of 2000 higher than 1,255 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00130390, the US trial registry maintained by the National Library of Medicine. NCT00130390 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.