Magnetic Resonance Imaging
Conditions
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
Sponsors
Study design
Intervention model description
Methodological development of new MRI approaches
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Spatial resolution of new MRI imaging sequences MRI scanning. | Two hours |
Countries
France