Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases
Completed
Conditions studied: Movement Disorders, Myoclonus, Nervous System Diseases, Tic Disorders, Tremor
In brief
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.
Key facts
- Study ID
- NCT00001667
- Run by
- National Institute of Neurological Disorders and Stroke (NINDS)
- People needed
- 300
- Starts
- 1997-03-01
- Expected to finish
- 2000-04-01
- Last updated by the study team
- 2008-03-04
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
Where it is running
- National Institute of Neurological Disorders and Stroke (NINDS) — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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