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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03152539
Acronym
MAP-VS
Enrollment
733
Registered
2017-05-15
Start date
2012-06-07
Completion date
2021-07-08
Last updated
2021-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Magnetic Resonance Imaging

Brief 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

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.

Interventions

RADIATIONMRI
DEVICEEEG
DEVICENIRS

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Methodological development of new MRI approaches

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Spatial resolution of new MRI imaging sequences MRI scanning.Two hours

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026