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Molecular genetics of familial heart disease

Molecular genetics of familial heart disease - Genetics of familial heart disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37798
Enrollment
300
Registered
2012-06-12
Start date
2012-06-12
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

congenital heart defect Congenital heart disease

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Individuals from families with two or more affected persons with congenital heart disease and/or (thoracic) aortic aneurysm are included. Affected family members as well as unaffected family members are included.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Genetic defects underlying CHD and aortic aneurysms.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)