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Earlier Diagnosis and Better Treatment Mission Related to the Cohort Programme
Sponsor: Luxembourg Institute of Health
Summary
The Luxembourg Parkinson's Study is an ongoing longitudinal nationwide monocentric observational study. It collects extensive clinical, molecular, genetic, and digital device-based longitudinal data, as well as foreseen post-mortem diagnostic validation (Hipp et al., 2018). The cohort consists of more than 1,600 participants from Luxembourg and the Greater Region, comprising patients with typical PD or atypical parkinsonism - irrespective of disease stage, age, cognitive status, comorbidities, or linguistic background - followed-up annually and age- and sex-matched healthy control subjects followed-up every 4 years. To provide a large, longitudinally followed, and deeply phenotyped set of patients and controls for clinical and fundamental research on PD, the investigators have implemented an open-source digital platform that has been partly harmonized with other international PD cohort studies. This effort is flanked by comprehensive biosampling efforts assuring high quality and sustained availability of body liquids and tissue biopsies (including blood, urine, stool, saliva, hair, skin biopsy and cerebrospinal fluid). All data and samples are stored, curated, and integrated into state-of-the-art data and biobank facilities.
Official title: Biomaterial Collection for Neurodegenerative Disease Research (ND Collection)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
1800
Start Date
2014-12-19
Completion Date
2025-12-31
Last Updated
2025-08-06
Healthy Volunteers
Yes
Conditions
Interventions
Observational study with sample and data collection
Observational study with sample and data collection
Locations (2)
Centre Hospitalier de Luxembourg (CHL), "Parkinson's Research Clinic"
Luxembourg, Luxembourg
Clinical and Epidemiological Investigation Center (CIEC)
Luxembourg, Luxembourg