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Clinical Trials in France / NCT05758961
Recruiting Observational

Le French Gut: Characterization of Gut Microbiota Profiles in France

NCT05758961 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2022-09-15
Last updated
2026-06-15

Condition(s) studied

General Population

Study summary

" The French Gut " is a national contribution aiming to collect 100,000 faecal samples and associated nutritional and clinical data by 2027. Le French Gut is initiated by MetaGenoPolis-INRAE, supported by INRAE with Prof. R. Benamouzig, (AP-HP) as principal investigator of the project. The main goal of this national trial is a better understanding of the observed heterogeneity between gut microbiome of healthy subjects, its connections with the diet and lifestyle, but also changes in gut microbiota associated with diseases (diabetes, obesity, allergies, cancer, Parkinson, Alzheimer…).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Persons over the age of 18 living in France. * Consent form signed electronically. Non inclusion Criteria: * Non-adult person (declarative); * Person not living in France (declarative); * Persons subject to a protective measure, in particular under guardianship or curatorship or unable to express their consent (declarative); * Person having had a colectomy (declarative); * Person with a digestive stoma (declarative); * Person who has not signed the consent; * Person who did not answer the entry questionnaire; * Person who has not sent a compliant stool sample; * Antibiotic intake in the 3 months before inclusion (declarative); * Performing a colonoscopy in the 3 months preceding inclusion (declarative).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre de Recherche sur Volontaire Bobigny France Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05758961 on ClinicalTrials.gov ↗ ← All trials in France