CHU Rennes
Rennes, 35000, France
Location status: Recruiting
Location contact
Blandine Gautier
CONTACT
Jean-Christophe Ferre, Pr
PRINCIPAL_INVESTIGATOR
NCT Number: NCT05107232
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.
Interested in participating?
Request Info6 year and older
All sexes
Interventional
Not applicable
Rennes, 35000, France
Location status: Recruiting
Blandine Gautier
CONTACT
Jean-Christophe Ferre, Pr
PRINCIPAL_INVESTIGATOR
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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
MRI
Time frame: 15 days
The quality of the images, maps or signals collected will be compared to standard acquisitions. This evaluation will be done by statistical comparison of visual qualitative criteria by expert radiologists or on quantitative criteria drawn from analyzes computing data obtained by processing experts images (signal-to-noise ratio, contrast-to-noise ratio, blur level, mutual information, co-location of regions highlighted by different techniques, etc.).
Contact information is provided by the study sponsor or research team.
Rennes University Hospital
Other
Acronym: OSV-IRM
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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