Trials / Completed
CompletedNCT02403765
Diagnostic Tools for Parkinson's Disease
Realization of Diagnostic Tools for the Early Analysis of Parkinson's Disease Through the Identification of Genetic Risk Profiles
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 500 (actual)
- Sponsor
- Neuromed IRCCS · Academic / Other
- Sex
- All
- Age
- 30 Years
- Healthy volunteers
- Accepted
Summary
The study aims to identify genetic variants associated to Parkinson's disease through the analysis of exome-sequencing data of familial cases and controls. The identified variants will be used to generate a diagnostic tool for the identification of genetic risk profiles.
Detailed description
1. Clinical evaluation of PD patients and relatives 2. High throughput analysis of genetic variants in genome exomes 3. Genotype-phenotype association testing 4. Identification of genetic risk variants for PD
Conditions
Timeline
- Start date
- 2015-05-01
- Primary completion
- 2018-10-01
- Completion
- 2019-10-31
- First posted
- 2015-03-31
- Last updated
- 2019-11-04
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT02403765. Inclusion in this directory is not an endorsement.