PROGENI (Parkinson's Research: The Organized Genetics Initiative) Family Study of LRRK2 (Leucine-rich Repeat Kinase 2)
Completed
Conditions studied: Parkinson Disease
In brief
The PROGENI Family Study is part of a larger consortium that is studying a gene shown to be important in Parkinson's disease, called LRRK2. People who have a defect in the LRRK2 gene will often develop Parkinson's disease. Eligible participants will be asked to complete a single Study Visit at an affiliated research facility closest to their home.
Key facts
- Study ID
- NCT01536821
- Run by
- Indiana University
- People needed
- 81
- Starts
- 2011-05-01
- Expected to finish
- 2013-12-01
- Last updated by the study team
- 2013-12-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Positive for a LRRK2 mutation
Where it is running
- Cleveland Clinic Florida — Weston, Florida, United States
- Indiana University Medical Center — Indianapolis, Indiana, United States
- University of Iowa Hospitals — Iowa City, Iowa, United States
- Kansas University Medical Center — Kansas City, Kansas, United States
- University of Maryland School of Medicine — Baltimore, Maryland, United States
- University of Nebraska — Omaha, Nebraska, United States
- Beth Israel Medical Center — New York, New York, United States
- Medical University of Ohio — Toledo, Ohio, United States
- Oregon Health & Science University — Portland, Oregon, United States
- University of Alberta — Edmonton, Alberta, Canada
Full record on ClinicalTrials.gov
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