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Optimization of magnetic resonance imaging (MRI) protocols on healthy volunteers and voluntary patients.
In MRI, a large number of technical parameters (sequence, parameters in sequence, antenna, reconstruction method, etc.) can be changed to optimize the diagnostic quality of the exam. Some optimizations can be performed on participants healthy volunteers, others need to be carried out on images pathological and acquired in voluntary patients.
Full description
An inclusion visit is planned to verify the criteria for selection, then an imaging visit to perform the MRI examination.
The imaging visit can take place at the end of the inclusion visit and until the following 15 days. For healthy volunteers, the visits are organized according to their availability. For patients, on the other hand, participation in the research will depend on the programming of the MRI within the framework care.
This is a single-center prospective study carried out at two sites in the Rennes University Hospital.
Enrollment
Sex
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Volunteers
Inclusion criteria
Criteria common to all participants:
Specific criteria for healthy volunteers:
o No medical or surgical history related to the anatomical area(s) scanned
Specific criteria for voluntary patients:
o Indication for an MRI exam as part of its management
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
600 participants in 1 patient group
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Central trial contact
Blandine Gautier; Jean-Christophe Ferre, Pr
Data sourced from clinicaltrials.gov
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