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Clinical Trials/NCT01429909
NCT01429909
Completed
Not Applicable

Optimization of fMRI for the Study of Basal Ganglia Activation in Parkinson's Disease: T2* Measurement in the Cortex and the Basal Ganglia

University Hospital, Clermont-Ferrand1 site in 1 country19 target enrollmentFebruary 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson's Disease
Sponsor
University Hospital, Clermont-Ferrand
Enrollment
19
Locations
1
Primary Endpoint
The quantitative measurement of T2* in the cortex and basal ganglia using MRI, made à J0.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Functional magnetic resonance imaging (fMRI) is a non-invasive imaging technique assessing neuronal activations during motor or cognitive tasks. The MRI sequences used are currently optimized for the study of cortex activations, particularly concerning the echo time (TE).Very few studies are interested in optimizing the fMRI for the study of the basal ganglia, structure implicated in many neurological diseases such as Parkinson's disease. The T2 * is a tissue parameter dependent of iron content, which differs with brain structures and probably also with age and in case of neurodegenerative disease. Optimal TE s should correspond to the T2 * of studied brain structure The primary purpose is to optimize the fMRI by a quantitative measurement of the T2* in the cortex and the basal ganglia using MRI. The secondary purpose is to study the effect of age and Parkinson's disease on T2*.

Detailed Description

80 subjects (40 PD patients and 40 paired healthy volunteers (on sex and age)) aged 40-80 years will be included. PD patients will be recruited in the Department of Neurology of CHU of Clermont-Ferrand. Healthy volunteers will be selected in clinical trial database. This study will consist of one visit (at J0) during which subjects will undergo a MRI (a single acquisition of 40 minutes approximately). PD patients will be further questioned on their disease and will benefit from a neurological examination

Registry
clinicaltrials.gov
Start Date
February 2011
End Date
December 2011
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Clermont-Ferrand
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • For patients :
  • Patients with idiopathic Parkinson's disease according to UKPDSBB criterias
  • Men or women aged between 40 to 80 years
  • not treated with deep brain stimulation
  • For healthy subjects
  • Men or women aged between 40 to 80 years

Exclusion Criteria

  • For patients
  • Dementia (MMS\<24)
  • Contraindication to MRI.
  • Under guardianship
  • In excluding period for another study
  • For healthy subjects
  • Antecedent of neurodegenerative diseases or psychiatric diseases
  • Contraindication to MRI
  • Under guardianship
  • In excluding period for another study

Outcomes

Primary Outcomes

The quantitative measurement of T2* in the cortex and basal ganglia using MRI, made à J0.

Time Frame: at day 1

Study Sites (1)

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