Trial Details

COMPLETED
Basic Information
Clinical ID c926
Identifier NCT05808023
Trial Title Dose-dependent FODMAP Reintroduction in IBS
Trial URL Visit Original Page
Study Information
Study Results

NO

Conditions Irritable Bowel Syndrome
Interventions OTHER: FODMAP powder reintroduction
Participant Information
Sponsor Universitaire Ziekenhuizen KU Leuven
City Bruges
Country/Region Belgium
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type INTERVENTIONAL
Phase NA
Time Information
Start Date 2023-04-01
Primary Completion Date 2025-08-25
Completion Date 2025-08-25