Diagnostic Tools for Parkinson's Disease

Status Completed

Clinical Trial 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.

Clinical Trial 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 ;

Study Design

Related Conditions & MeSH terms

Parkinson Disease

Clinical Trial Details

NCT number	NCT02403765
Study type	Observational
Source	Neuromed IRCCS
Contact
Status	Completed
Phase
Start date	May 2015
Completion date	October 31, 2019

View Details

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