Phase
Condition
N/ATreatment
Observational study with sample and data collection
Clinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Subjects with neurodegenerative disease or having Parkinson's disease (typical PD oratypical parkinsonism)
Subjects of all genders with a full capacity of consent
Subjects with a limited consent capacity if the legal guardian/authorisedrepresentative is in agreement
Subjects of at least 18 years of age at the time of inclusion
Exclusion
Exclusion Criteria:
Refusal to sign the informed consent
Limited capacity of consent on the part of the donor, if there is no legallydetermined guardian/authorised representative, or the latter is not present or doesnot agree with the inclusion
Active cancer
Pregnant women
Underage subjects of less than 18 years of age
Refusal to comply with mandatory sample collection
For invasive procedures, i.e., lumbar puncture and skin biopsy: relevant bloodclotting impairment, e.g., anamnestic evidence of frequent or prolonged bleedings.
Study Design
Connect with a study center
Centre Hospitalier de Luxembourg (CHL), "Parkinson's Research Clinic"
Luxembourg, 1210
LuxembourgActive - Recruiting
Clinical and Epidemiological Investigation Center (CIEC)
Luxembourg, 1445
LuxembourgActive - Recruiting
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