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Investigation of Vancomycin Efficacy in Patients With Ulcerative Colitis and Primary Sclerosing Cholangitis
Sponsor: McMaster University
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
Placebo (blinded)
Identical placebo capsule administered orally twice daily for 4 weeks.
Vancomycin (blinded)
Vancomycin 250 mg administered orally twice daily for 4 weeks.
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