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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05704413
Other study ID # APHP180540
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 17, 2021
Est. completion date September 17, 2026

Study information

Verified date January 2023
Source Assistance Publique - Hôpitaux de Paris
Contact Jérémie LEFEVRE, PU-PH
Phone +33 (0)1 49 28 25 63
Email jeremie.lefevre@aphp.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Constitution of a biobank of tissues, whole blood and plasma samples and stools to identify markers associated with treatment response, postoperative morbidity including neuro-cognitive and mood complications and prognosis of Inflammatory Bowel disease or colorectal cancer.


Description:

Inflammatory Bowel disease (Crohn, Ulcerative colitis) and colorectal cancer are frequent affections and the microbiota plays a major role in their physiopathology involving the immune system. In this setting, the interplay between gut microbiota and brain is still unexplored. To evaluate the interaction of the microbiota and the immune system with the host in these two chronic diseases, we aim to create a prospective biobank. A small amount of tissue will be taken during surgery. A whole blood, plasma and stoll samples will also be taken from the patient. All samples will be anonymized.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date September 17, 2026
Est. primary completion date September 17, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Ulcerative colitis, Crohn's disease or colorectal disease - Digestive resection with useless tissue available - Information consent signed Exclusion Criteria: - Patients < 18 years

Study Design


Locations

Country Name City State
France Service de Chirurgie Viscérale - Hôpital Saint Antoine Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relation between biological parameters and outcomes of digestive disease (IBD, CRC) identify relations between serumon response to treatment, postoperative outcomes including neuro-cognitive and mood complications and prognosis. up to 12 months after the incusion
Secondary Relation between biological parameters and outcomes of digestive disease (IBD, CRC) identify relations between plasma on response to treatment, postoperative outcomes including neuro-cognitive and mood complications and prognosis. up to 12 months after the incusion
Secondary Relation between biological parameters and outcomes of digestive disease (IBD, CRC) identify relations between DNA on response to treatment, postoperative outcomes including neuro-cognitive and mood complications and prognosis. up to 12 months after the incusion
Secondary Relation between biological parameters and outcomes of digestive disease (IBD, CRC) identify relations between faeces) on response to treatment, postoperative outcomes including neuro-cognitive and mood complications and prognosis. up to 12 months after the incusion
Secondary Exploratory study on the physiopathology of host-microbiota interactions to determinate the occurrence of intestinal and extra-intestinal complications genetic polymorphisms, serum markers, intestinal microbiota markers to determining the occurrence of intestinal and extra-intestinal complications up to two months after the incusion
Secondary Exploratory study on the physiopathology of host-microbiota interactions to determinate the response to treatments genetic polymorphisms, serum markers, intestinal microbiota markers determining : response to treatments up to two months after the incusion
Secondary Exploratory study on the physiopathology of host-microbiota interactions genetic polymorphisms, serum markers, intestinal microbiota markers determining : interactions between host and microbiota up to two months after the incusion
Secondary Brain-microbiota interaction Exploring the pathophysiology of host-microbiota interactions in postoperative cognitive or behavioral changes involving inflammation pathways up to two months after the incusion
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