Clinical Trials in France / NCT04645628
Recruiting
Not applicable
Optimization of the Acquisition Sequence to Improve the Quality and Comfort of Magnetic Resonance Imaging Exam
NCT04645628 · tracked via the Priya Life Science France tracker
Condition(s) studied
Healthy SubjectsPatient Performing an MRI Examination
Investigational drug(s) / intervention(s)
MRI examination
MRI examination: All subjects (healthy subjects and patients) will have an MRI examination with optimized sequences
Study summary
The purpose of this study is to evaluate the optimization of MRI acquisition sequences.
Eligibility
Inclusion Criteria for all subjects :
* to be over 18 year-old,
* to be able to understand the instructions given,
* to be enrolled in a social security plan,
* to have underwent a pre-inclusion medical examination,
* to give a written consent.
Inclusion Criteria especially for Patients :
* to perform a MRI examination of the head, neck, spine, thorax, abdomen, pelvis, retroperitoneum, lower limbs, upper limbs or whole body during clinical follow-up care.
Exclusion Criteria for all subjects :
* any contraindication to MR examination (active medical device, ferromagnetic foreign body, pregnancy, morbid obesity, claustrophobia, … ),
* subject under a measure of legal protection.
Exclusion Criteria especially for Healthy Subjects :
* to have a pathology in the anatomical area to be imaged
* to be employed by the CHRU of Nancy or having the slightest link of subordination with the CHRU of Nancy.
Exclusion Criteria especially for Patients :
* to have a limited MRI examination time due to a sensitive clinical situation (sedation, unstable hemodynamic state, postoperative).
Primary outcome measure(s)
- Image quality based on standard imaging quality criteria. — 6 months after the last inclusion
The image quality will be appreciated visually at least by a radiologist or a researcher.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHRU de Nancy | Nancy | France | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04645628 on ClinicalTrials.gov ↗ ← All trials in France