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NOT YET RECRUITING
NCT07341282
PHASE2

Investigation of Vancomycin Efficacy in Patients With Ulcerative Colitis and Primary Sclerosing Cholangitis

Sponsor: McMaster University

View on ClinicalTrials.gov

Summary

This clinical trial tests if oral vancomycin can safely treat active ulcerative colitis (UC) in adults who also have primary sclerosing cholangitis (PSC), a liver condition. The main questions it aims to answer are: * Can oral vancomycin improve UC symptoms as measured by Mayo score at 4 weeks? * Is oral vancomycin safe and tolerable in this patient group? Participants will be compared to see if vancomycin works better than placebo. Participants will: * Take oral vancomycin (250 mg twice daily) or identical placebo capsules for 4 weeks * Have the option for 4 more weeks of open-label vancomycin after the blinded phase * Attend clinic visits at baseline, week 4, and follow-up for Mayo scoring, endoscopy, blood/stool tests, and safety checks * Track treatment adherence and side effects The study primarily assesses if the trial can recruit 14 participants, retain them, achieve good adherence, and follow protocol procedures (feasibility). Secondary goals include safety (adverse events) and early signs of benefit in UC activity, liver tests, and gut bacteria balance. This pilot will guide larger future studies.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

14

Start Date

2026-01

Completion Date

2027-03

Last Updated

2026-01-14

Healthy Volunteers

No

Interventions

DRUG

Placebo (blinded)

Identical placebo capsule administered orally twice daily for 4 weeks.

DRUG

Vancomycin (blinded)

Vancomycin 250 mg administered orally twice daily for 4 weeks.

DRUG

Vancomycin (open-label extension)

Vancomycin 250 mg administered orally twice daily for 4 weeks (optional extension offered to both arms).

Locations (1)

McMaster Children's Hospital - Digestive Diseases Clinic

Hamilton, Ontario, Canada