Recruitment

Recruitment Status
Unknown status

Inclusion Criteria

older than 18, patients with IBS, patients with no organic disorders, patients informed and agreed to participate
older than 18, patients with IBS, patients with no organic disorders, patients informed and agreed to participate

Exclusion Criteria

patients with sclerodermia, diabetes, obesity, anorexia, colo-rectal surgery, patients with small intestinal bacterial overgrowth, pregnancy
patients with sclerodermia, diabetes, obesity, anorexia, colo-rectal surgery, patients with small intestinal bacterial overgrowth, pregnancy

Summary

Conditions
Irritable Bowel Syndrome
Type
Interventional
Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Masking: None (Open Label)
  • Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The main objective is to evaluate the efficacy of the FODMAPS diet on IBS symptoms and to correlate the results with the respiratory test

The main objective is to evaluate the efficacy of the FODMAPS diet on IBS symptoms and to correlate the results with the respiratory test

Inclusion Criteria

older than 18, patients with IBS, patients with no organic disorders, patients informed and agreed to participate
older than 18, patients with IBS, patients with no organic disorders, patients informed and agreed to participate

Exclusion Criteria

patients with sclerodermia, diabetes, obesity, anorexia, colo-rectal surgery, patients with small intestinal bacterial overgrowth, pregnancy
patients with sclerodermia, diabetes, obesity, anorexia, colo-rectal surgery, patients with small intestinal bacterial overgrowth, pregnancy

Tracking Information

NCT #
NCT02188680
Collaborators
Not Provided
Investigators
  • Principal Investigator: Anne-Marie LEROI, Professor University Hospital, Rouen
  • Anne-Marie LEROI, Professor University Hospital, Rouen