Observatory of Functionnal Digestive Disorders

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
France
Physiology Unit, Hopital Charles Nicolle, 1 rue de Germont
RECRUITING
Rouen
Contact Information
Primary
Anne-Marie AL LEROI, Professor
anne-marie.leroi@chu-rouen.fr
33232888990
Time Frame
Start Date: 2020-10-09
Estimated Completion Date: 2030-10-09
Participants
Target number of participants: 2000
Sponsors
Leads: University Hospital, Rouen

This content was sourced from clinicaltrials.gov