RecruitingNCT05266872

Earlier Diagnosis and Better Treatment Mission Related to the Cohort Programme

Biomaterial Collection for Neurodegenerative Disease Research (ND Collection)


Sponsor

Luxembourg Institute of Health

Enrollment

1,800 participants

Start Date

Dec 19, 2014

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is building a long-term patient registry (cohort) for people with Parkinson's disease or related movement disorders. The goal is to collect blood, urine, spinal fluid, and brain imaging data over time to understand how these conditions develop and improve diagnosis and treatment. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with Parkinson's disease (typical or atypical) - You are able to provide informed consent yourself, or a legal guardian can consent on your behalf **You may NOT be eligible if...** - You refuse to sign the consent form - You have active cancer - You are pregnant - You are unable to give consent and have no legal guardian available - You are unwilling to provide the required study samples Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERObservational 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

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NCT05266872


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