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Clinical Trial Summary

The goal of this observational study is to determine the factors associated with a delayed diagnosis and/or an immediately complicated disease for CD patients. A questionnaire will be completed by the patients, each questionnaire has a patient section and a physician section.


Clinical Trial Description

Number of patients expected : at least 600, coming from all types of practices (ANGH (expert hospitals), GETAID (expert university hospitals) and CREGG (expert private practice)). Recruitment period : 1 year Primary endpoint : The primary endpoint is the description of the factors linked to: - The IBD - The patient (see patient questionnaire in annex 1) - The health care system - The patient's self-care Secondary endpoint : - Validation of the "red flags" in a prospective cohort. - Comparison with the EPIMAD population, especially the location and severity. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06250361
Study type Observational
Source Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
Contact Charlotte Mailhat, PhD
Phone + 33 9 72 57 61 60
Email cmailhat@getaid.org
Status Not yet recruiting
Phase
Start date February 15, 2024
Completion date June 15, 2025

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