A Longitudinal Observational Follow-up of the PRECEPT Study Cohort (PostCEPT)
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ClinicalTrials.gov Identifier: NCT00605163
Recruitment Status : Unknown
Verified March 2008 by The Parkinson Study Group. Recruitment status was: Enrolling by invitation
First Posted : January 30, 2008
Last Update Posted : March 28, 2008
The Parkinson Study Group
National Institute of Neurological Disorders and Stroke (NINDS)
The purpose of this study is to longitudinally follow consenting clinical trial participants who participated in PRECEPT (A Randomized, Double Blind, Placebo Controlled, Dose Finding Study to Assess the Efficacy and Safety of CEP 1347 in Patients With Early Parkinson's Disease). The study will assess the clinical and imaging outcomes relevant to the natural history of Parkinson's disease (PD), as well as determine early biomarkers of the disease.
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Layout table for eligibility information
Ages Eligible for Study:
30 Years and older (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Parkinson disease patients who participated in the PRECEPT clinical trial.
Participation in the PRECEPT study
Willing and able to give informed consent
Patients will be excluded from participating in the the study if either of the criteria stated above is not met