Cure8

Why This Matters

Researchers tested whether adding a high-dose statin (atorvastatin 80 mg) to mesalamine improves quality of life for people with ulcerative colitis. If beneficial, a commonly used, inexpensive drug could offer a new adjunct approach for some patients not on immunosuppressives or biologics.

Who Should Pay Attention

Adults with ulcerative colitis (not on steroids, immunosuppressives, or biologics), gastroenterologists, IBD researchers, and clinicians interested in repurposing cardiovascular drugs for inflammatory disease.

Study Snapshot

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

What To Know

A Phase 2 interventional trial (completed) registered at ClinicalTrials.gov tested adding atorvastatin 80 mg daily to standard mesalamine (1 g three times daily) in adults with ulcerative colitis.

The trial planned about 50 participants and compared health-related quality of life (SF-36) at 6 months between the atorvastatin-plus-mesalamine group and a mesalamine-only control group. The registry entry highlights rationale: statins like atorvastatin have anti-inflammatory and immunomodulatory effects beyond cholesterol lowering.

Key exclusions included severe UC, current systemic or rectal steroids, immunosuppressives, biologics, significant liver/kidney dysfunction, pregnancy, and breastfeeding. This record reports study design and registered outcomes (HRQL by SF-36) but does not provide results or efficacy/safety findings in the provided text.

For outcome data or safety information, look for a results posting on ClinicalTrials.gov, a peer-reviewed publication from the study investigators, or contact the study site listed (Faculty of Medicine, Mansoura University).

Keep In Mind

This is a trial registry record (Phase 2, completed) describing study design and planned outcomes; the supplied text does not include trial results. Statins can affect liver enzymes and are contraindicated in significant liver disease, which aligns with the trial's exclusion criteria. Do not interpret this entry as evidence of benefit without seeing published outcome data.

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
SponsorTanta University
Trial IDNCT05561062
Study typeInterventional
Trial phasePhase 2
Enrollment50 participants
Indexed viaClinicalTrials.gov
Source typeTrial registry record
PublishedOct 30, 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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