Studies of the Variable Phenotypic Presentations of Rapid-Onset Dystonia Parkinsonism and Other Movement Disorders

Running, not enrolling

Conditions studied: Dystonia, Parkinsonism

In brief

The purposes of this study are to identify persons with rapid-onset dystonia-parkinsonism (RDP) or mutations of the RDP gene, document prevalence of the disease, and map its natural history.

Key facts

Study ID
NCT00682513
Run by
State University of New York at Buffalo
People needed
198
Starts
2008-04-01
Expected to finish
2027-07-31
Last updated by the study team
2026-05-06

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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