Skip to content

European Spinocerebellar Ataxia Type 3/Machado*Joseph Disease Initiative

European Spinocerebellar Ataxia Type 3/Machado*Joseph Disease Initiative - ESMI

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55616
Enrollment
35
Registered
2017-03-23
Start date
2017-05-01
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

cerebellar dysfunction disorder of coordination

Interventions

None listed

Sponsors

Neurologie
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients and carriers with SCA3 18 and older

Exclusion criteria

Exclusion criteria: Other neurological disorders Claustrofobia Metal prosthesis or other metal objects in body Implanted electronic devices such as a pacemaker

Design outcomes

Primary

MeasureTime frame
Main study parameters/endpoints: A large cohort of preclinical and mildly ataxic SCA3 mutation carriers, which includes a model of disease evolution in SCA3 and new clinical, motor, imaging and biochemical markers.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)