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Clinical Trials in France / NCT04918329
Recruiting Observational

Functional Digestive Disorders Observatory

NCT04918329 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2020-10-09
Last updated
2026-01-08

Condition(s) studied

Irritable Bowel SyndromeDyspepsiaFunctional ConstipationFaecal IncontinenceAbdominal Pain (AP)Vomiting Syndrome

Investigational drug(s) / intervention(s)

Observational study

Observational study: Non interventional study

Study summary

Functional digestive pathologies are defined by symptoms such as functional dyspepsia, gastroesophageal reflux, irritable bowel syndrome, gastroesophageal reflux, functional constipation, functional diarrhea, functional bloating, the opioid-induced constipation and fecal incontinence, without organic substratum. These diseases are very common in the general population (20%) and represent the first cause of consultation in city gastroenterology. The pathophysiology of these functional disorders is complex and often multifactorial: disturbances in digestive motility, altered visceral sensitivity, sphincter dysfunction, post-surgery, intestinal inflammation, dysbiosis, and impairment of the gut-brain axis. For example, it has been shown that one in four patients with inflammatory bowel disease in confirmed remission report digestive symptoms consistent with a functional bowel disorder, suggesting a possible pathophysiological continuum between these two conditions.

The objective of this study is to collect prospective clinical and tests data and a biological collection from biological samples (digestive biopsies, blood, urine and fecal samples) collected as part of the standard care. This collection could identify diagnostic or prognostic markers of the therapeutic response.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients over 18 years of age; * Patients with functional digestive disorder for more of 3 months; * Patients assessed as part of routine care; * Patients affiliated to the Social Security ; * Patients not opposed to participation in the Centre Exclusion Criteria: * Person deprived of liberty by administrative or judicial decision or major protected subject (under guardianship or curatorship); * Patients unable for any reason to read, understand, respond questionnaires (visual, psychiatric, cognitive, etc.)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Physiology Unit, Hopital Charles Nicolle, 1 rue de Germont Rouen France Recruiting

More University Hospital, Rouen trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04918329 on ClinicalTrials.gov ↗ ← All trials in France