Conotruncal Cardiac Defects and Nutrigenetic Etiopathogeny
NCT ID: NCT01460316
Last Updated: 2016-01-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
400 participants
OBSERVATIONAL
2011-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Conotruncal cardiac defects patients
Bood sampling for biochemicals and genetic analysis
There will be one blood sampling for the nutritionnal, metabolic and genetic parameters studied in the protocol
Mothers of patients
Bood sampling for biochemicals and genetic analysis
There will be one blood sampling for the nutritionnal, metabolic and genetic parameters studied in the protocol
Interventions
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Bood sampling for biochemicals and genetic analysis
There will be one blood sampling for the nutritionnal, metabolic and genetic parameters studied in the protocol
Eligibility Criteria
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Inclusion Criteria
* Weight: \> 3750 g
Exclusion Criteria
* 22q11 deletion Holder's
* Patients whose mother's took anti-folates before and during first pregnancy semester
1 Month
ALL
Yes
Sponsors
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Centre Hospitalier Universitaire de Besancon
OTHER
University Hospital, Strasbourg, France
OTHER
Centre Hospitalier Universitaire Dijon
OTHER
CHU de Reims
OTHER
Central Hospital, Nancy, France
OTHER
Responsible Party
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FEILLET François
Professor, M.D. Ph.D
Principal Investigators
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François FEILLET, MD-PHD
Role: PRINCIPAL_INVESTIGATOR
CHU de Nancy- Hôpital Brabois Enfants
Locations
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Service de Cardiologie Pédiatrique, CHU Brabois Enfants
Vandœuvre-lès-Nancy, , France
Countries
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Other Identifiers
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2011-A00346-35
Identifier Type: -
Identifier Source: org_study_id
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