NCT06291038 Efficacy of Glutamine Supplementation in Patients Suffering From Irritable Bowel Syndrome With Impaired Intestinal Permeability
| NCT ID | NCT06291038 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University Hospital, Rouen |
| Condition | Irritable Bowel Syndrome |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2024-10-03 |
| Primary Completion | 2029-03-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2024-10-03 with a primary completion date of 2029-03-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Irritable bowel syndrome (IBS) affects approximately 5% of the general population and remains a daily problem in the practice of clinicians with inconsistent effectiveness of treatments while patients' expectations are high. One of the functional abnormalities described during IBS is increased intestinal permeability. This increase in intestinal permeability is primarily present in the diarrheal subtype (IBS-D) and can be measured using the lactulose/mannitol test. Glutamine is a non-essential amino acid which regulates numerous metabolic pathways, and which plays a key role in the intestine because it is the preferential substrate of enterocytes and immune cells. Ex vivo, glutamine is able to restore the expression of tight junction proteins in patients suffering from IBS-D. On the other hand, glutamine supplementation is capable of reducing abdominal pain and restoring intestinal permeability disorders in a subgroup of patients with intestinal permeability disorder (post-infectious IBS-D). The working hypothesis would be that all patients suffering from IBS with permeability disorder, measured by the lactulose/mannitol test, could benefit from oral glutamine supplementation.
Eligibility Criteria
Inclusion Criteria: * Adult aged 18 to 75 * Diarrheal irritable bowel syndrome (IBS-D), according to the Rome IV criteria (appendix 2) * Francis score \> 175/500 at inclusion (corresponding to moderate to severe IBS) * Treatments for IBS stable for \>1 month * Affiliation to a social security system * Adult person having read and understood the information letter and signed the consent form * Woman of childbearing age having effective/very effective contraception (Cf. CTFG) (estrogen-progestins or intrauterine device or tubal ligation) for 1 month and a negative urine pregnancy test * Postmenopausal woman: confirmatory diagnosis (amenorrhea not medically induced for at least 12 months before the inclusion visit or biologically documented) Exclusion Criteria: * Taking probiotics, anti-inflammatories, corticosteroids or antibiotics systemically (oral or injectable) in the month preceding the study and during the duration of the study treatment, * Known diagnosis of active autoimmune disease (type 1 diabetes, lupus, multiple sclerosis, thyroiditis, ankylosing spondylitis, rheumatoid arthritis or psoriasis) * Known allergy to glutamine, * Contraindication to taking glutamine, protein powder, lactulose or mannitol (including sugar-free chewing gum), * Use of osmotic laxatives and/or taking lactulose and/or protein supplementation (including taking glutamine) in the 4 weeks preceding the start of the study, * Renal insufficiency (GFR\<40mL/min), hepatic insufficiency (PT\<70) or known heart disease, * ATCD of digestive disease (celiac disease, chronic inflammatory bowel disease, abdominal surgery other than appendectomy or cholecystectomy), * Occlusive or subocclusive syndrome, * Digestive perforation or suspicion of perforation, * Abdominal pain syndrome of undetermined cause, * Chronic alcohol consumption (\>14 units/week), * Pregnant or parturient or breastfeeding woman or proven absence of contraception, * Person deprived of liberty by an administrative or judicial decision or person placed under judicial protection/under guardianship or curatorship, * Person participating in research participating in another trial / having participated in another trial within 2 weeks, * History of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol or preventing them from giving informed consent.
Frequently Asked Questions
Who can join the NCT06291038 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Irritable Bowel Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06291038 currently recruiting?
Yes, NCT06291038 is actively recruiting participants. Visit ClinicalTrials.gov or contact University Hospital, Rouen to inquire about joining.
Where is the NCT06291038 trial being conducted?
This trial is being conducted at Amiens, France, Caen, France, Le Havre, France, Rouen, France.
Who is sponsoring the NCT06291038 clinical trial?
NCT06291038 is sponsored by University Hospital, Rouen. The trial plans to enroll 60 participants.