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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05842564
Other study ID # 69HCL21_1020
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 2023
Est. completion date September 2025

Study information

Verified date April 2023
Source Hospices Civils de Lyon
Contact Rémi DUCLAUX-LORAS, MD, PhD
Phone 0472357050
Email remi.duclaux-loras@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Crohn's disease is a multifactorial complex disease resulting in a between microbiota and immune system. Indeed, GWAS (Genome-Wide Association Studies) association study pinpointed polymorphisms as genes susceptibility on more than 200 loci. Among them genes coding for proteins involved in autophagy machinery (i.e: ATG16L1, IRGM et NDP52). Autophagy is a ubiquitous intracellular mechanism mandatory for protein and microorganism recycling. So far, the role of autophagy in gut inflammation and intestinal homeostasis in Crohn's disease patients is partially understand. Then, investigators plan to evaluate, on native cells, the autophagic flux in pediatric patients suffering of a Crohn's disease compare to controls.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 70
Est. completion date September 2025
Est. primary completion date June 2025
Accepts healthy volunteers No
Gender All
Age group 6 Years to 17 Years
Eligibility Inclusion Criteria: For Crohn's Disease group : - Age between 6 and 17 inclusive - Patients with a weight > 25 kg at the time of inclusion - Patients with Crohn's disease requiring ileocolonoscopy (diagnosis or follow-up) - Mild to severe Crohn's disease consistent with PCDAI disease activity score - Patients on nutritional therapy (Modulen/Modulife), corticosteroids, salicylic derivatives, immunosuppressants, biotherapies (anti-TNF, vedolizumab and ustekinumab) or without treatment - Consent form signed by the patient or the holder(s) of parental authority. - Affiliation to a social security scheme or beneficiaries of a similar scheme. For Control group: - Between 6 and 17 years old included - Presenting a weight > 25 kg at the time of inclusion - Without a diagnosis of Crohn's disease - Requiring evaluation by ileoendoscopy - Consent form signed by the patient or the holder(s) of parental authority. - Affiliation to a social security scheme or beneficiaries of a similar scheme. Exclusion Criteria: - Refusal to participate in the protocol - Intercurrent infection - Ongoing antibiotic treatment - Patient involved in another interventional study protocol including an exclusion period still in progress at pre-inclusion - Pregnant, parturient or breastfeeding women (on questioning) - Persons deprived of their liberty by a judicial or administrative decision - Persons subject to psychiatric care - Persons admitted to a health or social establishment for purposes other than research

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Blood samples
Blood sample of maximum 20ml (5 tubes of EDTA of 4ml or 5 tubes of EDTA of 2ml and a tube for the conservation of genomic DNA)
Biopsies
5 biopsies (one for each segment of the intestine explored: ileum, right colon, transverse colon left colon and sigmoid) will be taken during the ileocolonoscopy

Locations

Country Name City State
France Service Hépatologie, Gastroentérologie et Nutrition pédiatrique, Hôpital Femme Mère Enfant, HCL Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quantification of autophagic flux by western blot. LC3II/LC3I will be measured by western blot after booking the autophagic flux at different time point. 1 day (during hospitalization for ileocolonoscopy)
Secondary Incidence of autophagic polymorphisms in pediatric Crohn's disease population DNA sequencing of polymorphisms reported in the literature as gene mutations susceptibility for Crohn's disease. 1 day (during hospitalization for ileocolonoscopy)
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