National Parkinson Foundation Patient Registry Protocol

Brief description of study

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. This study will be enrolling any person who receives medical care for the diagnosis of idiopathic Parkinson's disease at any of the participating Centers.


Clinical Study Identifier: s16-01357
Principal Investigator: Andrew S. Feigin
Currently Recruiting

Contact the research team to learn more about this study.


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