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OSV-IRM - Volunteer MRI Sequence Optimization

R

Rennes University Hospital

Status

Enrolling

Conditions

MRI

Treatments

Other: MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT05107232
35RC21_8958_OSV-IRM

Details and patient eligibility

About

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

600 estimated patients

Sex

All

Ages

6+ years old

Volunteers

Accepts Healthy Volunteers

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:

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

    • 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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

600 participants in 1 patient group

Participants
Other group
Description:
Patients and Healthy volunteers included will have an MRI
Treatment:
Other: MRI

Trial contacts and locations

1

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Central trial contact

Blandine Gautier; Jean-Christophe Ferre, Pr

Data sourced from clinicaltrials.gov

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