Development of MRI Protocols and Associated Explorations (EEG, NIRS) in Voluntary Patients
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 48
- Locations
- 2
- Primary Endpoint
- Spatial resolution of new MRI imaging sequences MRI scanning.
Study 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.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Basic Science
- Masking
- None
Masking Description
Magnetic resonance imaging
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts 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
Outcomes
Primary Outcomes
Spatial resolution of new MRI imaging sequences MRI scanning.
Time Frame: Two hours
Secondary Outcomes
No secondary outcomes reported