Preclinical Evaluation of Multimodal Therapeutic Strategies in Intestinal Irradiation and Inflammatory Bowel Disease From Organoids

NCT ID: NCT05425901

Last Updated: 2025-09-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-19

Study Completion Date

2024-12-11

Brief Summary

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This study is carried out in patients with IBD and healthy subjects requiring ileocolonoscopy as part of routine care (disease monitoring or polyp/colon cancer screening). It aims the generation and culturing of organoids from digestive biopsies recovered from healthy and/or pathological (inflammatory) ileal and/or colonic mucosa during an ileo-colonoscopy. These cultures will make it possible to validate the organoid production method used in the context of the research (primary objective). In a second phase (secondary objectives), the study will aim to setup a screening tool by irradiating the organoids (step one) and then evaluate in vitro the regenerative activity of treatments dedicated to improve inflammatory bowel diseases and acute radiation enteritis (step two).

Detailed Description

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Conditions

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Radiation Enteritis Inflammatory Bowel Diseases

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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IBD

active or quiescent

Group Type EXPERIMENTAL

biopsy

Intervention Type OTHER

endoscopy biopsies (6)

control

polyp screening

Group Type ACTIVE_COMPARATOR

biopsy

Intervention Type OTHER

endoscopy biopsies (6)

Interventions

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biopsy

endoscopy biopsies (6)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

\- Group 1: active IBD

* 18 years old or older
* Assured IBD diagnosis (Crohn's disease/ulcerative colitis) according to European Crohn's and Colitis Organisation (ECCO) 2019 consensus criteria
* Active IBD (Harvey-Bradshaw score of 4 or above for Crohn's disease or partial Mayo score of 3 or above for ulcerative colitis)
* Indication to perform a coloscopy
* Written consent for study participation obtained

Or

\- Group 2: inactive IBD

* 18 years old or older
* Assured IBD diagnosis (Crohn's disease/ulcerative colitis) according to ECCO 2019 consensus criteria
* Inactive IBD (Harvey-Bradshaw score below 4 for Crohn's disease or partial Mayo score below 3 for ulcerative colitis)
* Indication to perform a coloscopy
* Written consent for study participation obtained

Or

\- Group 3: Control

* 18 years old or older
* Indication to perform a coloscopy to detect polyp
* No known bowel disease
* Written consent for study participation obtained

Exclusion Criteria

* Inability to understand, read, sign informed consent and/or express consent
* Person subject to legal protection (curator, guardianship or safeguard of justice),
* Deprivation of liberty by judicial or administrative decision,
* Non-affiliation to a social security scheme or non-beneficiary of such a scheme
* Pregnant, parturient, breastfeeding women
* Contraindication to performing biopsies
* Participation in other therapeutic research that may modify the behavior of intestinal cells (for example, drug research for the treatment of IBD)
* Anticoagulant treatment or bleeding disorder
* Person subject to a judicial safeguard measure
* People hospitalized without consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Research Agency, France

OTHER

Sponsor Role collaborator

Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Groupe Hospitalier Ambroise Paré Hartmann

Neuilly-sur-Seine, Hauts-de-Seine, France

Site Status

Countries

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France

Other Identifiers

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2021-A02973-38

Identifier Type: REGISTRY

Identifier Source: secondary_id

C20-53

Identifier Type: -

Identifier Source: org_study_id

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