Irritable Bowel Syndrom (IBS) K58.9
Conditions
Interventions
Group 1: 36 patients with IBS (18 with IBS-D and 18 with IBS-C) receive after antibiotic pretreatment 3 allogeneic FMTs via colonoscopy or sigmoidoscopy. Changes of clinical symptoms is elicited using
Sponsors
Klinische Abteilung für GastroenterologieMedizinische Universität Graz
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients with IBS, aged between 18 and 80 years, informed consent
Exclusion criteria
Exclusion criteria: -) Secondary gastrointestinal motility disorder, -) Major abdominal surgery, -) Pregnant and lactating women, -) Medication under another clinical trial, -) Serious chronic diseases such as neoplasia, autoimmune disorders or metabolic disorders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective is to evaluate whether allogeneic FMT has a positive impact on clinical scores in IBS after 90 days. | — |
Secondary
| Measure | Time frame |
|---|---|
| -) Improvement of stool frequency and consistency of the Bristol-stool-scale. -) Change in intestinal microbiota -) Change the methane content of the exhaled air in the lactulose / CH4 breath test -) Subgroup analysis IBS-D and IBS-O. | — |
Countries
Austria
Contacts
Public ContactPatrizia Kump
Klinische Abteilung für GastroenterologieMedizinische Universität Graz
Outcome results
None listed