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

Conditions
atherosclerosis
cardiovascular disease
10007510
10003216
Registration Number
NL-OMON33048
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
1000
Inclusion Criteria

Member of high penetrence family for cardiovascular disease

Exclusion Criteria

None

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>A) Identification of sequence variations resulting in CVD in pedigrees<br /><br>B) Determining through which mechanism sequence variations result in disease.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>none</p><br>
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