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The PASS-PD study is set out to screen individuals from the general population with an increased risk for the development of Parkinson's Disease (PD) and to investigate this highly enriched cohort longitudinally for five year. A special focus is placed on implementation of ethical standards for early risk disclosure in PD.
The PASS-PP Study is designed to combine the latest developments in clinical and biomarker research to 1. understand the distribution of risk profiles for PD in the general population, especially regarding non-motor symptoms 2. identify subjects with a likelihood of developing PD 3. follow individuals with a high likelihood/risk to develop PD in the future (compared to individuals with low risk and) in a prospective study 4. understand the potential of biological markers to increase prediction of progression/conversion 5. identify subtypes of PD patients, by providing a detailed clinical phenotyping with a main focus on non-motor symptoms cluster 6. provide a framework of ethical handling of early risk disclosure in PD
Age
50 - 99 years
Sex
ALL
Healthy Volunteers
Yes
Department for Neurology, University of Kiel
Kiel, Germany
Start Date
June 1, 2021
Primary Completion Date
December 1, 2027
Completion Date
December 1, 2027
Last Updated
September 22, 2025
2,000
ESTIMATED participants
No intervention
OTHER
Lead Sponsor
University Hospital Schleswig-Holstein
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06113640