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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.
Full 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:
Secondary endpoint :
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Central trial contact
Charlotte Mailhat, PhD
Data sourced from clinicaltrials.gov
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