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Dose-dependent FODMAP Reintroduction in IBS — DORI  

Irritable Bowel Syndrome Clinical Trial

Official title:
Dose-dependent Individual FODMAPs (Mannitol and Fructans) Reintroduction in Patients With Irritable Bowel Syndrome

Clinical Trial Summary

The aim of this study is to evaluate whether symptom recurrence, after successful FODMAP elimination, is dose-dependent in patients with IBS. The effect of a blinded reintroduction of FODMAP powders fructans and mannitol will be investigated in a crossover dose-escalation scheme for the identification of the eliciting dose in individual patients. The reintroduction of FODMAPs is performed after a successful elimination by the LFD.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05808023
Study type Interventional
Source Universitaire Ziekenhuizen KU Leuven
Contact Jan Tack
Phone 016 34 42 18
Email jan.tack@kuleuven.be
Status Recruiting
Phase N/A
Start date April 2023
Completion date December 2024
View Details
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