NCT01730599UnknownNot Applicable
A Longitudinal 5 Years Follow up Study in Parkinson's Disease (PD) Patients Carriers of the LRRK2 Gene G2019S Mutation
Tel-Aviv Sourasky Medical Center1 site in 1 country200 target enrollmentStarted: November 2012Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- change from baseline in updrs motor and total scores
Study Overview
Brief Summary
This is a longitudinal study in patients with Parkinson's Disease (PD) carriers of a genetic mutation - substitution of gly with ser in position 2019 (G2019S) in the leucine-rich repeat kinase 2 (LRRK2) gene. The purpose of this study is to explore the association between genetic mutations in the known genes and their influence on disease manifestation over few years of follow up
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
Eligibility Criteria
- Ages
- 30 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •parkinson'd disease patients that already participated in a pasr cross sectional study
Exclusion Criteria
- •subjects with cognitive decline by the parameters defined in Diagnostic and Statistical Manual of Mental Disorders (DSM)- IV
- •subjects with psychiatric disorder
- •subjects unable to sign a consent form
Outcomes
Primary Outcomes
change from baseline in updrs motor and total scores
Time Frame: the participants will be followed for 5 years. the measurements will be taken evry 18 month.
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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