Trials / Unknown
UnknownNCT03440983
OSS-IRM: Optimization of MRI Sequences in Healthy Volunteers
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 600 (estimated)
- Sponsor
- Rennes University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
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.
Detailed 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | MRI data acquiring 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 |
Timeline
- Start date
- 2013-04-01
- Primary completion
- 2021-12-01
- Completion
- 2022-12-01
- First posted
- 2018-02-22
- Last updated
- 2018-09-28
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT03440983. Inclusion in this directory is not an endorsement.