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Gene mutations and -variations in congenital heart defects

Gene mutations and -variations in congenital heart defects - Gene mutations and -variations in congenital heart defects

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31069
Enrollment
160
Registered
2007-10-09
Start date
2007-08-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

congenital cardiovascular malformation congenital heart defect

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Patients with a congenital heart defect, with a variant in the DNA. 2) First degree relatives of patients with a congenital heart defect with a variant in the DNA.

Exclusion criteria

Exclusion criteria: 1) Patients with a congenital heart defect, without a variant in the DNA.

Design outcomes

Primary

MeasureTime frame
A genetic variation in relatives, with or without congenital heart defects, of patients with a congenital heart defect and a proven genetic variation. Occurrence of (mild) congenital heart defects in relatives, with or without the genetic variation found in de index patient, of patients with a congenital heart defect and a proven genetic variation.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)