Trials / Completed
CompletedNCT00001667
Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 300 (planned)
- Sponsor
- National Institute of Neurological Disorders and Stroke (NINDS) · NIH
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this protocol is to identify families with inherited neurologic conditions, especially movement disorders, to evaluate affected and unaffected individuals clinically, and to obtain blood samples for genetic analysis.
Detailed description
The purpose of this protocol is to identify families with inherited neurologic conditions, especially movement disorders, to evaluate affected and unaffected individuals clinically, and to obtain blood samples for genetic analysis.
Conditions
Timeline
- Start date
- 1997-03-01
- Completion
- 2000-04-01
- First posted
- 2002-12-10
- Last updated
- 2008-03-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00001667. Inclusion in this directory is not an endorsement.