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…
- clinical presentation consistent with ATP1A3 disease (RDP, AHC) or confirmed diagnosis of RDP or AHC
You may not qualify if…
- none
Where it is running
- University of Miami — Miami, Florida, United States
- University at Buffalo — Buffalo, New York, United States
Full record on ClinicalTrials.gov
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