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

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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON47371

Enrollment

400

Registered

2015-03-25

Start date

2015-11-10

Completion date

Unknown

Last updated

2025-09-01

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

Conditions

familial amyloid angiopathy HCHWA-D

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria: Age

Design outcomes

Primary

Measure	Time frame
Number of HCHWA-D mutation carriers, their disease expression and other genetic, environmental and vascular risk factors that could influence their disease course.	—

Countries

Netherlands

Outcome results