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NCT03152539 Clinical Trial

Development of MRI Protocols and Associated Explorations (EEG, NIRS) in Healthy Volunteers

Magnetic Resonance Imaging Clinical Trial

— MAP-VS  

Official title:
Development of MRI Protocols and Associated Explorations (EEG, NIRS) in Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03152539
Other study ID # 38RC12.238
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 7, 2012
Est. completion date July 8, 2021

Study information
Verified date October 2021
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of the studies that will be carried out on volunteer patients who have given their consent will be the development and optimization of the sequence parameters or the design of the stimulation paradigms in order to optimize the quality and Relevance of the images realized taking into account anatomical, functional or metabolic parameters. These adjustments will be carried out without interfering with the management of voluntary patients

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.

Recruitment information / eligibility
Status Completed
Enrollment 733
Est. completion date July 8, 2021
Est. primary completion date July 8, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - major - socially insured persons - given their consent. - absence of contraindication to the MRI examination Exclusion Criteria: - Subjects under the age of 18 - pregnant women - all other persons referred to in articles L1121-5 to L1121-8 of the CSP

Study Design

Related Conditions & MeSH terms

Intervention

Radiation:
• MRI

Device:
• EEG

• NIRS

Locations
Country Name City State
France CHU Grenoble-Alpes Grenoble

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Spatial resolution of new MRI imaging sequences MRI scanning. Two hours
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