Irritable Bowel Syndrome Regional Cohort
Development of a Regional Irritable Bowel Syndrome Cohort
University Hospital, Rouen
600 participants
Mar 4, 2025
OBSERVATIONAL
Conditions
Summary
Setting up a regional (multicentre), longitudinal cohort of people suffering from irritable bowel syndrome followed up in consultation to study the natural history of the disease and its prognosis.
Eligibility
Inclusion Criteria5
- Patient
- Normal laboratory work-up as part of routine care (CBC, CRP)
- Over 18 years of age
- Patient affiliated to a social security scheme
- Person who has read and understood the information letter and does not object to taking part in the study
Exclusion Criteria5
- Patient suffering from an organic digestive pathology (chronic inflammatory bowel disease, microscopic colitis when endoscopy has been performed because deemed necessary, digestive cancer, coeliac disease) or major digestive surgery (excluding appendectomy and cholecystectomy).
- Patient refusal
- Patient does not speak or understand French
- A pregnant woman or a woman in labour or breastfeeding
- Person deprived of liberty by an administrative or judicial decision or person placed under court protection / sub- guardianship or curatorship
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Interventions
Patients will fill in these self-questionnaires on a tablet or on paper, depending on the availability of tablets in the centres, before and after consulting the doctor. These questionnaires assess the severity of the disease and quality of life.
Stool samples will be taken at each visit, i.e. approximately every 6 months for patients
Locations(4)
View Full Details on ClinicalTrials.gov
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NCT06900491