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Taking people in EgyptPhase 2/3

Nitazoxanide Added to Usual Care for Mild-to-Moderate Ulcerative Colitis

Tests nitazoxanide alongside standard care versus placebo in adults with ulcerative colitis.

Plain-language title generated from the registry record
Registry title: Nitazoxanide as Adjunct Therapy in Mild-to-Moderate Ulcerative Colitis

Key facts

Where
Tanta, EgyptSee the site
Phase
Phase 2/3

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18-65 with mild-to-moderate ulcerative colitis who have been on stable treatment. It tests nitazoxanide added to standard therapy over 12 weeks.

Age
18 to 65 years
Sex
All sexes can join
Disease stage
Ulcerative colitis confirmed for at least 6 months, with mild-to-moderate active disease (Mayo score 3-10)
Earlier treatment
Stable ulcerative colitis treatment for at least 8 weeks before joining. No antibiotics, probiotics or investigational drugs within 4 weeks. No recent start or dose change of a biologic.

Main reasons for not taking part

  • Severe or fulminant ulcerative colitis needing hospital care or surgery
  • Active intestinal infection, for example C. difficile
  • Severe liver, kidney or heart disease, or cancer
  • Pregnancy or breastfeeding
  • Known allergy to nitazoxanide

Read by machine on 10 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07820046, who can take part

Where in Egypt

  • Tanta University HospitalTanta, EgyptTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Tanta University
Trial code
NCT07820046
Record updated
9 November 2026
Original description
Ulcerative colitis (UC) is a chronic inflammatory bowel disease characterized by relapsing inflammation of the colonic mucosa. Despite advances in therapeutic options, many patients experience incomplete remission or treatment resistance. Emerging evidence suggests that intestinal barrier dysfunction, microbiota dysbiosis, and immune dysregulation play central roles in UC pathogenesis.Read full original descriptionShow less

Nitazoxanide in Mild-to-Moderate Ulcerative Colitis: A Randomized, Double-Blind, Placebo-Controlled Trial

Ulcerative colitis (UC) is a chronic inflammatory bowel disease characterized by relapsing inflammation of the colonic mucosa. Despite advances in therapeutic options, many patients experience incomplete remission or treatment resistance. Emerging evidence suggests that intestinal barrier dysfunction, microbiota dysbiosis, and immune dysregulation play central roles in UC pathogenesis.

Nitazoxanide is a broad-spectrum antiparasitic agent with demonstrated antimicrobial, anti-inflammatory, and immunomodulatory effects, including inhibition of NF-κB signaling and improvement of intestinal barrier integrity. Preclinical studies suggest potential benefit in experimental colitis models; however, clinical evidence remains limited.

This randomized, double-blind, placebo-controlled trial aims to evaluate the efficacy and safety of nitazoxanide as an adjunct to standard therapy in patients with mild-to-moderate ulcerative colitis over a 12-week treatment period.

Inclusion: Age 18-65 years; Confirmed ulcerative colitis ≥ 6 months; Mild-to-moderate active disease (Mayo score 3-10); Stable UC therapy ≥ 8 weeks before enrollment Exclusion Criteria; Severe/fulminant UC requiring hospitalization or surgery; Active intestinal infection (e.g., C. difficile); Antibiotics/probiotics/investigational drugs within 4 weeks; Recent biologic initiation or dose change; Severe hepatic, renal, cardiovascular disease, or malignancy; Pregnancy or lactation; Known hypersensitivity to nitazoxanide.

ClinicalTrials.gov NCT07820046