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Identification of the molecular basis of premature atherosclerosis in high penetrance pedigrees

Identification of the molecular basis of premature atherosclerosis in high penetrance pedigrees - PAS PEDIGREES

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33048
Enrollment
1000
Registered
2009-09-15
Start date
2009-06-01
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

atherosclerosis cardiovascular disease

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Member of high penetrence family for cardiovascular disease

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
A) Identification of sequence variations resulting in CVD in pedigrees B) Determining through which mechanism sequence variations result in disease.

Secondary

MeasureTime frame
none

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)