The Stool Microbiome of Treated and Untreated IBS (Irritable Bowel Syndrome) Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorWeizmann Institute of Science

About this trial

Irritable bowel syndrome (IBS) is considered the most common gastrointestinal disorder in humans, with an estimated global prevalence of 11%-20% of all humans. Alterations in the gut microbiome are at the center of IBS, and microbiome-induced volatile metabolites in response to dietary exposures is believed to drive a downstream impact on susceptible hosts, thereby driving the disease. However, the characteristics and functions of these metabolites remain unknown to date. The two main mechanisms invoking IBS development and flares include 1) an increase in luminal water content due to malabsorption of small molecules and 2) incrementation of colon gas production generated by the fermentation of small molecules by gut bacteria.Yet to date, a person-specific elucidation of the specific small molecules and bacteria driving IBS, and their downstream effects on the human gut epithelium remain unknown.

Over the past years, it became evident that dietary regimes, and their interactions with the intestinal microbiome, are at the center of IBS symptom generation and alleviation. The most widely used dietary intervention is a highly restrictive diet, the low-Fermentable Oligo-saccharides Di-saccharides Mono-saccharides And Polyols (FODMAP) diet, based on avoidance of multiple food items that contain available fermentable molecules.

The low-FODMAP diet remains an effective line of treatment for IBS patients, yet due to its complexity and unhealthy nature, it remains a last line of treatment and fails to impact the majority of IBS patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Male and Female

Age - 18-70

Disqualifiers

Consumption of antibiotics 2 months prior to the first day of the experiment.

Consumption of probiotic supplements 1 month prior to the first day of the experiment.

Type 1 or type 2 diabetes diagnosis.

Pregnancy, fertility treatments, breastfeeding 3 months prior to the first day of the study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Low FODMAP dietary regimen

    Other intervention

    intervention will include a guidance by a clinical dietitian about low FODMAP diet The FODMAP diet has three phases: 1. Elimination - Avoidance from high-FODMAP foods (2-6 weeks) 2. Reintroduction -Structured challenges of specific food groups each time (6-8 weeks). 3. Maintenance - personalized diet, according to the response in step 2.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Non-IBSNo intervention 0 interventions
Group B: IBS -low FODMAPExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

IBS-SSS - irritable bowel syndrome severity score system questionnaire

Severity of symptoms as they are scored in the Rome IV IBS-SSS 75 to \<175 to indicate mild IBS, 175 to \<300 as moderate, and \>300 as severe

Time frame
1 week
2

IBS-QOL questionnaire - irritable bowel syndrome quality of life questionnaire

Quality of life scores from the Rome IV IBS-QOL 0-100 scale for ease of interpretation with higher scores indicating better IBS specific quality of life

Time frame
1 week

Secondary outcomes

1

Stool microbiome differences between the study arms - using fecal samples of participants

Analysis of stool samples of the different study arms - using shot-gun metagenomics to asses type of microbiota pre and post low-FODMAP diet.

Time frame
3 months

Other outcomes

Sponsors and contacts

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