The CAA-HERITAGE study: Hereditary Cerebral Amyloid Angiopathy-Dutch type; Investigating Genealogy and Disease Course

Recruiting

• Conditions: 10047075; familial amyloid angiopathy; HCHWA-D; 10029299; 10007963

• Registration Number: NL-OMON47371
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 400

Inclusion Criteria

Age >=18 years
Diagnosed with: HCHWA-D with proven mutation; and/or symptoms suggestive of the mutation.
Ability and willingness to provide written informed consent.

Exclusion Criteria

Age < 18 years
Inability to give informed consent or obtain informed consent from a legal representative

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Number of HCHWA-D mutation carriers, their disease expression and other<br /><br>genetic, environmental and vascular risk factors that could influence their<br /><br>disease course.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>not applicable </p><br>