Parkinson's Disease Clinical Trial
Official title:
Parkinson's Disease Registry
The purpose of the Parkinson's disease Registry is to develop a national and international
database of persons with Parkinson's disease (PD). The Registry will be used to facilitate
the development of new therapies and healthcare services to improve the quality of life for
people with PD. It will also be a means for investigators in the field of PD to quickly
identify and notify subjects about other research studies for which they are eligible.
Objectives include:
- Assess current treatment approaches and develop best-practice guidelines
- Track the functional abilities, access to healthcare and cost of illness of people with
PD over time
- Drive the development of innovative research projects
- Accelerate the process of informing patients of research projects for which they may be
eligible
Status | Active, not recruiting |
Enrollment | 20000 |
Est. completion date | December 2015 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Clinical diagnosis of Parkinson's disease Exclusion Criteria: - No clinical diagnosis of Parkinson's disease |
Observational Model: Ecologic or Community, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Muhammad Ali Parkinson Research Center | Phoenix | Arizona |
Lead Sponsor | Collaborator |
---|---|
Muhammad Ali Parkinson Research Center | Barrow Neurological Foundation |
United States,
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---|---|---|---|
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