NL-OMON47377
Recruiting
Not Applicable
Genetic Origin of Congenital Heart Disease Identification of genetic variants causing congenital heart disease - GO Heart study
niversitair Medisch Centrum Utrecht0 sites1,050 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Congenital Heart Disease
- Sponsor
- niversitair Medisch Centrum Utrecht
- Enrollment
- 1050
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Patient has Congenital Heart Disease
- •\- Patient undergoes an invasive procedure (cardiac catheterization or cardiac surgery) during which DNA can be obtained
Exclusion Criteria
- •(1\) No informed consent obtained for present study.
- •(2\) Patients that do not allow to be informed about unexpected genotypic findings to which known treatments are available.
- •(3\) No informed consent for blood sample drawing by one of the parents for NGS
- •(4\) Patient is a monozygotic twin.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Recruiting
Not Applicable
ew genetic approaches in congenital heart diseasecongenital heart defectcongenital heart disease1001039410007510NL-OMON50751Academisch Medisch Centrum915
Withdrawn
Not Applicable
Molecular Basis of Congenital Heart DefectsCongenital Heart DefectsNCT00579358University of California, Irvine
Not yet recruiting
Not Applicable
Gene mutations and -variations in congenital heart defectscongenital cardiovascular malformationcongenital heart defect1001039410007510NL-OMON31069Academisch Medisch Centrum160
Completed
Not Applicable
Cardio-Genetic Basis of Sudden Infant Death Syndrome occurring in Temporal Association with Vaccinatiocot death and cardiac sodium channelopathies1000752110007510NL-OMON37517Academisch Medisch Centrum22
Completed
Not Applicable
Molecular genetics of familial heart diseasecongenital heart defectCongenital heart disease1001039410007510NL-OMON37798Academisch Medisch Centrum300