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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02851134 |
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Date of registration:
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07/06/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Search for New Genetic Mutations Major Effect in Crohn's Disease
MC-WES |
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Scientific title:
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Search for New Genetic Mutations Major Effect in Crohn's Disease |
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Date of first enrolment:
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April 2015 |
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Target sample size:
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20 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02851134 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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France
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Contacts
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Name:
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Corinne Gower, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University Hospital, Lille |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Crohn disease subject
- EPIMAD family with, at least, 3 Crohn disease subjects
Exclusion Criteria:
- Pregnant or lactating women
Age minimum:
5 Years
Age maximum:
80 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Crohn Disease
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Intervention(s)
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Biological: blood and stools samples
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Genetic: genetic analysis
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Primary Outcome(s)
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NOD2 gene status
[Time Frame: 8 months after recruiting]
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Secondary Outcome(s)
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Whole Exome Sequencing
[Time Frame: 10 months after recruiting]
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Secondary ID(s)
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2013_53
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2014-A00023-44
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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