Study Description: The purpose of the Registry is to collect data on individuals with Parkinson?s disease to better understand the illness and ultimately improve the care and survival of those individuals with the disease. The Patient Registry may also be used to initiate and design clinical research studies that will test new or existing treatments and may result in new treatments for future patients.
Principal Investigator: John Morgan
Eligibility Criteria: diagnosis of idiopathic Parkinson?s disease
Compensation: No, subjects will not be compensated.
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