Trial Details
Not RecruitingBasic Information
| Clinical ID | c2144 |
|---|---|
| Identifier | CTIS2023-507425-42-00 |
| Trial Title | A Prospective, Randomized, Placebo-controlled Clinical Trial of oral vancomycin in adults and young adults (15-17 years old) affected by Primary Sclerosing Cholangitis with or without Inflammatory Bowel Disease - VanC-IT |
| Trial URL | Visit Original Page |
Study Information
| Study Results | No results available |
|---|---|
| Conditions | Primary Sclerosing Cholangitis MedDRA version: 20.1Level: LLTClassification code: 10036732Term: Primary sclerosing cholangitis Class: 10019805;Therapeutic area: Diseases [C] - Digestive System Diseases [C06];MedDRA version: 20.1Level: LLTClassification code: 10036732Term: Primary sclerosing cholangitis Class: 10019805 |
| Interventions | Product Name: , Product Code:SCP32734155, Pharmaceutical Form: , Other descriptive name: , Strength: , Product Name: Placebo capsules contain the only excipient present in the formulation, Polyethylene glycol 6000; the active ingredient is substituted by the same excipient to obtain the intended filling weight. The pharmaceutical form is white/white 00 hard gelatin capsules for oral administration., Product Code:N/A, Pharmaceutical Form: N/A, Other descriptive name: N/A , Strength: , Pharmaceutical form of the placebo: N/A |
Participant Information
| Sponsor | University Of Milano Bicocca |
|---|---|
| City | - |
| Country/Region | Italy |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | ADULT, CHILD, INFANT, OLDER_ADULT, TEENAGER |
Study Design
| Study Type | Interventional clinical trial of medicinal product |
|---|---|
| Phase | PHASE2 |
Time Information
| Start Date | 2025-04-24 |
|---|---|
| Primary Completion Date | - |
| Completion Date | - |