fecal bacteriotherapy K51
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient: chronic active UC with indication to total colectomy, age >18 and <80, informed consent. Donor: infomed consent
Exclusion criteria
Exclusion criteria: Patient: oral anticoagulation, coagulopathy, pregnancy. Donor: any severe disease (infection, malignancy, autoimmune idsease), any kind of diarrhoea, GI infections or any intestinal disease, antibiotic therapy within the last 6 month.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is a sustained reduction of at least 2 points in the MAYO score. Time points of clinical visitation performed by the principal investigator incl. MAYO score, blood tests and endoscopy are day 3,10, 30 and 90. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoint is a sustained chance of intestinal microbiota in patients with chronic activity of UC due to fecal bacteriotherapy. | — |
Countries
Austria
Contacts
Klinische Abteilung für Gastroenterologie und Hepatologie Medizinische Universität Graz