OSV-IRM - Volunteer MRI Sequence Optimization

  • STATUS
    Recruiting
  • End date
    Dec 20, 2027
  • participants needed
    600
  • sponsor
    Rennes University Hospital
Updated on 20 November 2021
Accepts healthy volunteers

Summary

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.

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.

Details
Condition Magnetic Resonance Imaging
Treatment MRI
Clinical Study IdentifierNCT05107232
SponsorRennes University Hospital
Last Modified on20 November 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Criteria common to all participants
Minor or major subject
Affiliated, himself or through his parents if he is a minor, to a a social security scheme
Having given their free, informed and written consent, and/or which the free, informed and written consent of the holder(s) parental authority has been obtained for minors
Specific criteria for healthy volunteers
No medical or surgical history related to the anatomical area(s) scanned
Specific criteria for voluntary patients
Indication for an MRI exam as part of its management

Exclusion Criteria

\- Contraindication to an MRI (pacemaker or pacemaker, neurostimulator, intra-orbital metal body, vascular clip ferromagnetic)
Pregnancy
Legal protection measure for adults in progress (safeguard of justice, guardianship, curatorship) or subject deprived of liberty
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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