Trial Details
RECRUITINGBasic Information
| Clinical ID | c638 |
|---|---|
| Identifier | NCT06291038 |
| Trial Title | Efficacy of Glutamine Supplementation in Patients Suffering From Irritable Bowel Syndrome With Impaired Intestinal Permeability |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| Conditions | Irritable Bowel Syndrome |
| Interventions | DIETARY_SUPPLEMENT: • Experimental group: treatment with glutamine at a dose of 5g 3 times a day for 8 weeks|DIETARY_SUPPLEMENT: • Control group: treatment with a protein powder (Protifar) (Placébo) 5g 3 times a day for 8 weeks. |
Participant Information
| Sponsor | University Hospital, Rouen |
|---|---|
| City | Amiens |
| Country/Region | France |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | NA |
Time Information
| Start Date | 2024-10-03 |
|---|---|
| Primary Completion Date | 2029-03-01 |
| Completion Date | 2029-03-01 |