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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00169364
Other study ID # P011104
Secondary ID
Status Recruiting
Phase N/A
First received September 12, 2005
Last updated August 28, 2007
Start date May 2002

Study information

Verified date September 2005
Source Groupe Hospitalier Pitie-Salpetriere
Contact Alexis Brice, MD, PhD
Phone 33-142162183
Email brice@ccr.jussieu.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

Parkinson's disease is a frequent neurodegenerative disorder. Genetic forms of the disease have been recently identified. The monogenic form due to parkin mutation is responsible for many familial cases and sporadic forms. However, the relationship between the mutation and the genotype of patients is not fully established. The aim of this study is to compare clinical, metabolic and neuropsychological characteristics obtained in patients with parkin mutation with those of patients without parkin mutation.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Juvenile Parkinson's disease (< 45 years)

- Parkin mutation

- Normal brain magnetic resonance imaging (MRI)

Exclusion Criteria:

- Contraindication to brain MRI

- Women without effective contraception

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
positron emission tomography


Locations

Country Name City State
France Centre d'Investigation Clinique-Hôpital Pitié-Salpetriere Paris

Sponsors (2)

Lead Sponsor Collaborator
Groupe Hospitalier Pitie-Salpetriere Délégation Régionale à la Recherche Clinique

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Parkin mutation
Primary Motor disability
Primary Neuropsychological evaluation
Primary Psychiatric evaluation
Secondary Positron emission tomography
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