LRRK2, GBA and Other Genetic Biomarkers in Eastern European (Ashkenazi) Jews With and Without Parkinson's Disease
NCT04668898 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 203
Last updated 2025-04-16
Summary
Single site observational study focused on elucidating the genes and biochemical pathways involved in causing Parkinson disease.
Conditions
- Parkinson Disease
- LRRK2
- GBA Gene Mutation
Sponsors & Collaborators
-
Massachusetts General Hospital
collaborator OTHER -
National Institute of Neurological Disorders and Stroke (NINDS)
collaborator NIH -
Icahn School of Medicine at Mount Sinai
lead OTHER
Principal Investigators
-
Rachel Saunders-Pullman, MD, MPH · Icahn School of Medicine at Mount Sinai
-
Laurie Ozelius, PhD · Massachusetts General Hospital
Eligibility
- Min Age
- 30 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2019-04-01
- Primary Completion
- 2025-04-01
- Completion
- 2025-04-01
Countries
- United States
Study Locations
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