A European Study to identify the needs of individuals and families affected by Juvenile Huntington's Disease

A European Study to identify the needs of individuals and families affected by Juvenile Huntington's Disease - Juvenile Huntington's Disease

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON30947

Enrollment

Registered

2007-07-18

Start date

2007-03-01

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

Huntington's disease in childhood

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: families with a patient with diagnosed juvenile Hungton's disease (onset under 18 years)

Exclusion criteria

Exclusion criteria: absence of informed consent

Design outcomes

Primary

Measure	Time frame
none	—

Secondary

Measure	Time frame
none	—

Countries

Netherlands

Outcome results