Active — Not RecruitingNot Applicable

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

United States198 participantsStarted 2008-04

Plain-language summary

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.

Who can participate

SexALL

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Inclusion Criteria: * clinical presentation consistent with ATP1A3 disease (RDP, AHC) or confirmed diagnosis of RDP or AHC Exclusion Criteria: * none

What they're measuring

RDP Severity

Timeframe: Visit 1 (baseline)

Trial details

NCT IDNCT00682513

SponsorState University of New York at Buffalo

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-07-31

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