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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03160235

Acronym

MAP-PV

Enrollment

Registered

2017-05-19

Start date

2013-02-01

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

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.

Interventions

RADIATIONMagnetic resonance imaging

DEVICEEEG

DEVICENIRS

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

BASIC_SCIENCE

Masking

NONE

Masking description

Magnetic resonance imaging

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 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

Design outcomes

Primary

Measure	Time 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