Cure8

Why This Matters

This trial tests whether adding the oral antibiotic nifuroxazide to standard mesalamine improves quality of life for people with mild-to-moderate ulcerative colitis. Results, if published, could suggest a new adjunctive treatment option.

Who Should Pay Attention

Adult patients with mild-to-moderate ulcerative colitis, gastroenterologists and IBD clinicians, and researchers interested in drug repurposing or antibiotic approaches for IBD.

Study Snapshot

Story typeClinical Reference
Trial phasePhase 2, Phase 3
Enrollment50 participants
Study statusCompleted
Source depthTrial registry record

What To Know

This is a ClinicalTrials.gov record for a completed Phase 2/3 interventional study (NCT05988528) testing nifuroxazide added to standard mesalamine versus mesalamine alone in adults with mild-to-moderate ulcerative colitis.

The trial planned to enroll about 50 participants at Tanta University (Egypt) and treated patients for 6 months, with the primary outcome listed as change in IBDQ health-related quality of life. The intervention arms list mesalamine 1 g three times daily for all participants and the experimental arm adds nifuroxazide 200 mg twice daily.

Key eligibility limits included ages 18–60 and exclusion of severe UC, steroid or biologic/immunosuppressive use, and certain comorbidities. Registry status in the record is marked COMPLETED.

If you’re reading this because you or someone you care for has UC, this entry describes a registered clinical study of an oral antibiotic (nifuroxazide) given alongside mesalamine — it reports the study design and planned outcomes, not study results or treatment recommendations.

For questions about whether this approach is appropriate, talk with your treating clinician.

Keep In Mind

This entry is a trial registry record (Phase 2/3, listed as COMPLETED) and contains design and eligibility details rather than published trial results. Nifuroxazide is described here as an oral antibiotic; the record does not provide outcome data in this extract. Confirmed efficacy and safety would require peer-reviewed results.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Clinical trial Evidence type derived from source or registry metadata.
PublicationClinicalTrials.gov
SponsorMostafa Bahaa
Trial IDNCT05988528
Study typeInterventional
Trial phasePhase 2, Phase 3
Enrollment50 participants
Indexed viaClinicalTrials.gov
Source typeTrial registry record
PublishedOct 13, 2026, 12:00 AM
Content availableTrial registry record

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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