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Single-center Exploratory Study of the Intestinal Microbiota in Patients Treated for Irritable Bowel Syndrome With Predominant Constipation and Methane Production

Recruitingn/aAges 18 Years - anyAllHospices Civils de Lyon
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In plain words

What the trial is, and whether it could suit you

Irritable Bowel Syndrome (IBS), characterized by the Rome IV criteria, is a functional bowel disorder combining abdominal pain with changes in bowel habits and/or stool consistency. This condition is common, affecting 5% to 10% of the population in developed countries. The etiology of IBS is multifactorial, involving intestinal motility disorders, visceral hypersensitivity, micro-inflammation of the intestinal mucosa, and dysbiosis. It has been demonstrated that the sub-category of IBS patients with constipation predominantly have increased amounts of Methanobrevibacter smithii, the most common methanogenic archaea found in the intestinal lumen, compared to other IBS patients. Breath tests can evaluate methane production by the intestinal microbiota, indirectly assessing the presence and quantity of methanogenic archaea. The acronym IMO (intestinal methanogen overgrowth) defines the as

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patient suffering from Irritable Bowel Syndrome (IBS) (abdominal pain for the past 6 months occurring on average at least 1 day per week in the last 3 months, with at least 2 of the following criteria: associated with defecation, associated with a change in stool frequency, associated with a change in stool consistency): 1. Predominant constipation type (IBS-C): Bristol Stool Scale 1-2 ≥ 25% of the time and Bristol Stool Scale 6-7 ≤ 25% of the time 2. Alternating diarrhea-constipation type (IBS-M): Bristol Stool Scale 1-2 25% of the time and Bristol Stool Scale 6-7 25% of the time 3. Unspecified type: absence of sufficient criteria to meet criteria for IBS-C, IBS-D, or IBS-M. * Patient exhibiting a high methane level (≥ 10 ppm) during a glucose breath test. * Aged ≥ 18 years at the time of study entry. * Patient not opposing participation in the study. Exclusion Criteria: * Patient who has been treated with antibiotics or probiotics in the last 3 months prior to inclusion. * Patient suffering from diarrhea-predominant IBS (Bristol Stool Scale 6-7 ≥ 25% of the time and Bristol Stool Scale 1-2 ≤ 25% of the time). * Patient with a history of abdominal surgery other than appendectomy and cholecystectomy. * Patient with a history of celiac disease. * Patient with proven inflammatory bowel disease. * Patient with a history of colorectal cancer. * Patient with uncontrolled hypothyroidism. * Patient with uncontrolled diabetes. * Pregnant or breastfeeding women. * Patient deprived of liberty by a judicial or administrative decision. * Adult patient under legal protection (guardianship, curators). * Patient unable to discontinue proton pump inhibitor treatment during the study period
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What it tests

  • Plasma Sample
  • Stool Sample
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Where

1 site
Hôpital Edouard Herriot
Lyon, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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