OSS-IRM: Optimization of MRI Sequences in Healthy Volunteers

R

Rennes University Hospital

Status

Unknown

Conditions

Healthy

Treatments

Device: MRI data acquiring in healthy volunteers

Study type

Interventional

Funder types

Other

Identifiers

NCT03440983
2011-A01531-40 (Other Identifier)

Details and patient eligibility

About

Using MRI, many technical parameters can be changed to optimize the diagnostic quality of the examination. The study is interventionnal because healthy volunteers are not supposed to have an MRI exam. The primary objective of this study is to optimize the imaging protocols and to validate the choice of the technical parameters in healthy volunteers. The quality of the images, cartographies or spectres will be compared to standard acquisitions. This evaluation will be based on qualitative visual criteria assessed by expert radiologists or on quantitative criteria assessed by data processing tools.

Full description

Using MRI, many technical parameters (sequence, parameters in the sequence, reconstruction method, etc.) can be changed to optimize the diagnostic quality of the examination. The primary objective of this study is to optimize the imaging protocols and to validate the choice of the technical parameters in healthy volunteers. The quality of the images, cartographies or spectres will be compared to standard acquisitions. This evaluation will be based on qualitative visual criteria assessed by expert radiologists or on quantitative criteria assessed by data processing tools. Prospective, single-center, observational MRI study A screening visit is planned to check the inclusion/non inclusion criteria followed by an imaging visit during which the MRI examination will be performed. Theses 2 visits are scheduled at the subject's convenience. The number of participations to the study is limited to 5 per year per subject.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or female subject,
  • Aged 18 or above

Exclusion criteria

  • Patient with any surgical clip, external clips, or any other ferromagnetic device, that is contraindicated for use in MRI
  • Claustrophobic patient
  • Pregnancy
  • Breastfeeding
  • Patients subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty
  • No healthcare insurance

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

600 participants in 1 patient group

MRI data acquiring in healthy volunteers
Experimental group
Description:
MRI data acquiring in healthy volonteers
Treatment:
Device: MRI data acquiring in healthy volunteers

Trial contacts and locations

1

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Central trial contact

drc drc; Jean-Christophe Ferré

Data sourced from clinicaltrials.gov

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