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Clinical Trials/NCT03160235
NCT03160235
Completed
Not Applicable

Development of MRI Protocols and Associated Explorations (EEG, NIRS) in Voluntary Patients

University Hospital, Grenoble1 site in 1 country48 target enrollmentFebruary 1, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Magnetic Resonance Imaging
Sponsor
University Hospital, Grenoble
Enrollment
48
Locations
1
Primary Endpoint
Spatial resolution of new MRI imaging sequences MRI scanning.
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Studies that will be carried out on healthy volunteers will have as main objective the development and optimization of the parameters of sequences or the design of the paradigms of stimulation in order to optimize the quality and the relevance of the images realized taking in Taking account of anatomical, functional or metabolic parameters, or integrating new approaches resulting from technical evolutions

Detailed Description

The pathologies that interest us in these refinements concern mainly the chronic (or sequellar) brain disorders which can be degenerative, developmental or vascular. The patients who will be recruited will be known patients of our Service (University Clinic of Neuroradiology and MRI) that we follow during checks. The type of examination that will be applied to them, between MRI, EEG and NIRS, will be specified in the consent form. These examinations will not be invoiced either to the patient or to the social security, and the related costs will be borne by our Federative Research Structure or sometimes, when these explorations are upstream of a defined research protocol and funded, They will be financed under this protocol.

Registry
clinicaltrials.gov
Start Date
February 1, 2013
End Date
July 8, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Grenoble
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • major voluntary patients
  • socially insured.
  • Karnofsky score above 60%.
  • given their consent.
  • absence of contraindication to the MRI examination

Exclusion Criteria

  • Subjects under the age of 18
  • pregnant women
  • persons referred to in articles L1121-5 to L1121-8 of the CSP.
  • Patients with acute illness

Outcomes

Primary Outcomes

Spatial resolution of new MRI imaging sequences MRI scanning.

Time Frame: Two hours

Study Sites (1)

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