Intestinal Permeability and Intestinal Microbiota in Irritable Bowel Syndrome

Phase 4

• Conditions: Irritable Bowel Syndrome With Diarrhea
• Interventions: Drug: prescribing anapproved drug, examination

• Registration Number: NCT05379036
• Lead Sponsor: I.M. Sechenov First Moscow State Medical University

Brief Summary

Patients with diarrhea-predominant irritable bowel syndrome (IBS) and functional dyspepsia (FD) were examined and received treatment in the study. Severity of complaints and quality of life patients were assessed according to questionnaires. The state of the intestinal barrier (analysis of the protein composition, intestinal mucin levels in biopsies, serum zonulin level in blood), the composition of the gut microbiota (16S rRNA gene sequencing), bacterial metabolic function (short-chain fatty acid levels in feces), and the presence of gut inflammation (levels of lymphocytes and eosinophils in biopsies) were assessed in the patients. Patients were divided into 3 treatment groups: trimebutin + placebo, rebamipide + placebo, trimebutin + rebamipide. The above parameters were compared in patients before and after treatment.

Detailed Description

The study included 60 patients with an established diagnosis IBS and FD. Patients were randomized in toone of three groups. Patients in group 1 received Trimedat (trimebutine, marketing authorization number LP-005534/07 of 2007-12-28) for 2 months, patients in group 2 received Trimedat and Rebagit (rebamipide, marketing authorization number LP-001831 of 2012-09-12) for 2 months, patients in group 3 received Rebagit for 2 months. The patients were blinded to the treatment assignment. At inclusion and 1 month after the severity of complaints were assessed, 2 months after starting treatment, the severity of complaints, quality of life, state of tight junction proteins, mucin-2 expression level, serum zonulin level, histological investigation of the mucous membrane of the small and large intestine, state of the intestinal microbiota and short-chain fatty acid levels were assessed. After the end of the study, an interim analysis of the effect of the therapy on the parameters was carried out. In the case of a positive effect, a full analysis of all the aforementioned factors contributing to its development was to be performed.

In addition, all these parameters were also in the control group (15 healthy volunteers without complaints, matched for sex and age with the main group).

Study Timeline

• Study Start: 2021-06-23
• Status Verified: 2022-03
• Study First Submitted: 2022-03-31
• Study First Submitted QC: 2022-05-12
• Last Update Submitted: 2022-05-12
• Study First Posted: 2022-05-18
• Last Update Posted: 2022-05-18
• Primary Completion: 2022-05-31
• Study Completion: 2022-05-31

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Signed informed consent
• A man or woman aged 18-59.
• For women of childbearing age: mandatory use of contraceptive methods.
• Confirmed diagnosis of IBS-D and functional dyspepsia by clinical, instrumental and blood chemistry findings (according to the Clinical Guidelines of the Russian Gastroenterological Association and the Russian Association of Coloproctologists (2016)
• Absence of Helicobacter Pylori infection according to the urea breath test in the past 6 months before inclusion.
• Ability to understand and willingness to comply with all protocol details.

Exclusion Criteria

• Prematurely discontinuation of the consumption of tested drugs/placebo;
• Started taking antibiotics, other probiotics, or prebiotics during the follow-up period;
• Refusal to participate during the follow-up period, including refusal to come for re-examination 2 months after inclusion;
• Cancer or inflammatory bowel disease diagnosis during the follow-up period.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group B	prescribing anapproved drug, examination	a group of patients who, after the examination, were prescribed therapy with rebamipide 300 mg per day for 2 months
Group A	prescribing anapproved drug, examination	a group of patients who, after the examination, were prescribed therapy with trimebutine 600 mg per day for 2 months
Group C	prescribing anapproved drug, examination	a group of patients who, after the examination, were prescribed therapy with trimebutine 600 mg per day + rebamipide 300 mg per day for 2 months

Primary Outcome Measures

Name	Time	Method
Severity of complaints	change from baseline points of questionnaires at 2 months	The severity of complaints is assessed using "7×7" (7 symptoms per 7 days) questionnaire and GSRS (Gastrointestinal Symptom Rating Scale)
Low-grade inflammation	change from baseline numbers of eosinophils and lymphocytes at 2 months	In biopsies of the small and large intestine, numbers of eosinophils and lymphocytes in the field of view were assessed by histological examination with hematoxylin-eosin staining

Secondary Outcome Measures

Name	Time	Method
Serum zonulin	baseline	The level of the permeability marker, serum zonulin, is assessed by enzyme-linked immunosorbent assay using an ELISA test kit (Immundiagnostik AG, Bensheim, Germany)
Mucin-2 expression	baseline	The level of Mucin-2 expression in biopsies of the small and large intestine is assessed by immunohistochemistry
Short-chain fatty acids	baseline	Short-chain fatty acid levels in feces are assessed by gas chromatography-mass spectrometry
Adverse events	2 months after the start of the study	Patients are notified of the need to report any adverse and unintended signs (any unfavourable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product)
Low-grade inflammation	baseline	In biopsies of the small and large intestine, numbers of eosinophils and lymphocytes in the field of view were assessed by histological examination with hematoxylin-eosin staining
Tight junction protein level	baseline	In biopsies of the small and large intestine, tight junction proteins levels are assessed by two-dimensional electrophoresis
Severity of complaints	baseline	The severity of complaints is assessed using "7×7" (7 symptoms per 7 days) questionnaire and GSRS (Gastrointestinal Symptom Rating Scale)
Gut microbiome	baseline	The composition of the gut microbiota in feces is analyzed by 16S rRNA sequencing
Quality of life (general health, limitation of activities, physical health problems, emotional health problems, social activities, pain, energy and emotions, social activities, general health)	change from baseline points of questionnaire levels at 2 months	Quality of life ((general health, limitation of activities, physical health problems, emotional health problems, social activities, pain, energy and emotions, social activities, general health) was assessed using the 36-Item Short Form Survey (SF-36) questionnaire

Trial Locations

Locations (1)

Elena Poluektova; 🇷🇺 Moscow, Russian Federation