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Chronic Intestinal Pathologies Analytical Cohort at TouLouse

Chronic Intestinal Pathologies Analytical Cohort at TouLouse

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04896684
Acronym
CAPITOL
Enrollment
300
Registered
2021-05-21
Start date
2021-04-29
Completion date
2025-09-30
Last updated
2024-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon Cancer, Inflammatory Bowel Diseases

Keywords

Intestinal Bowel syndrome, Inflammatory Bowel Disease, colon cancer screening, data and biological collection

Brief summary

In the general population, the percentage of people with at least one digestive disease is 16.7%. Among these digestive diseases, inflammatory bowel disease (IBD), irritable bowel syndrome (IBS) and patients who should benefit from digestive examinations as part of a screening oriented either by the patient's family history or following the performance of an immunological screening test ( FIT) in the stool will be studied. The aim of this project is to build a biological collection with associated clinical data for research projects.

Detailed description

In the general population, the percentage of people with at least one digestive disease is 16.7%. Among these digestive diseases, two of them namely inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS) will be more particularly studied. This interest is based on the increasing frequency of these two pathologies, their chronicities but above all the limited physiopathological data available. In addition, it seems interesting to study a third population, namely patients who should benefit from digestive examinations as part of a screening oriented either by the patient's family history or following the performance of an immunological screening test ( FIT) in the stool. The study of this population is part of an improvement in knowledge on the carcinogenesis of colorectal cancer. To study these populations, blood, serum, plasma and tissues from colonous biopsies or surgical samples will be collected. This cohort will make it possible to study, among other things, the pathophysiology of chronic diseases of the small intestine and the colon (IBD, IBS, screening) in order to improve their management through the development of new biomarkers and therapeutic targets.

Interventions

BIOLOGICALblood and intestinal biopsy sampling

24 mL of blood and 10 intestinal biopsies will be sampled

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Patient requiring endoscopic explorations for screening or follow-up in the context of a suspected IBS or IBD or colorectal cancer Or * Patient with IBD requiring surgical management * Patient over 18 years old * Patient able to read and understand the information leaflet * Patients who have given their consent to participate in the study * Patients affiliated to a social security system (including AME)

Exclusion criteria

* Patients who have received antibiotic treatments in the 10 days preceding endoscopic exploration * Pregnant or breastfeeding patients * Patients under 18 years old * Patients under guardianship or curatorship * Patients unable to sign a free and informed consent

Design outcomes

Primary

MeasureTime frameDescription
Biological collection associated with clinical dataBaselineSet up a biological collection associated with clinical data on main intestinal tract diseases in order to understand their physiopathology

Secondary

MeasureTime frameDescription
Identify new potential therapeutic moleculesBaselineAssessment of new treatment on organoids made thanks to intestinal biopsies
Optimize treatment success rates for IBDBaselineAssessment of new treatment on organoids made thanks to intestinal biopsies

Countries

France

Contacts

Primary ContactBarbara Bournet, MD, PhD
bournet.b@chu-toulouse.fr5 61 32 32 35
Backup ContactCindy Canivet
canivet.c@chu-toulouse.fr5 61 32 20 48

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026