Last updated: January 19, 2024
Sponsor: Benjamin Misselwitz
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
N/AClinical Study ID
NCT06191224
BASEC 2023-00706
Ages 18-90 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Signed informed consent
- Age 18-90 years
- General ability to give consent for study inclusion, understand and follow studyprocedures
- No current or past diagnosis of IBD or colorectal carcinoma
- No current medical complaints typical for IBD or other severe intestinal diseases (e.g. Diarrhea, severe constipation, abdominal pain, blood in stool, weight loss).Minor symptoms, (not impairing daily activities) are permitted.
- No other current relevant gastrointestinal disease or condition plausibly interferingwith microbiota assessment according to the discretion of the study physician.
Exclusion
Exclusion Criteria:
- All patients with recent acute gastrointestinal disease (e.g., confirmed infectiousdiarrhea) within the last month or relevant intestinal symptoms (impairing dailyactivities).
- Use of antibiotics within the last 3 months.
- Current pouch or ileostomy/ colostomy.
- Severe medical, surgical, or psychiatric comorbidities interfering with studyprocedure according to the judgement of the investigator (patients with comorbiditiesthat would not interfere with the primary endpoints I-III but don't allow theassessment of HRV according to the judgement of the investigator (e.g. heart diseases)will be included in the study but the HRV will not be assessed).
- Participation in an interfering clinical study.
Study Design
Total Participants: 200
Study Start date:
May 28, 2023
Estimated Completion Date:
July 05, 2025
Study Description
Connect with a study center
Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Switzerland
Bern, 3010
SwitzerlandActive - Recruiting
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