Search for New Genetic Mutations Major Effect in Crohn's Disease

NCT02851134 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2019-02-28

No results posted yet for this study

Summary

This study highlight genetics mutations with major effect in Crohn's Disease (CD) by WES in individuals affected and healthy individuals from EPIMAD Inserm InVS registry families.

Conditions

  • Crohn Disease

Interventions

GENETIC

genetic analysis

genetic (Whole Exome Sequencing )

BIOLOGICAL

blood and stools samples

biological collection

Sponsors & Collaborators

  • University Hospital, Lille

    lead OTHER

Principal Investigators

  • Corinne Gower, MD, PhD · University Hospital, Lille

Eligibility

Min Age
5 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2018-04-30
Completion
2018-04-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02851134 on ClinicalTrials.gov