Improving MRI Exam Quality and Comfort
Optimization of the Acquisition Sequence to Improve the Quality and Comfort of Magnetic Resonance Imaging Exam
NA · Central Hospital, Nancy, France · NCT04645628
This study is testing new ways to make MRI scans more comfortable and produce better images for both healthy people and patients needing these exams.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 720 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Central Hospital, Nancy, France (other) |
| Locations | 1 site (Nancy) |
| Trial ID | NCT04645628 on ClinicalTrials.gov |
What this trial studies
This study aims to optimize the acquisition sequences used during Magnetic Resonance Imaging (MRI) exams to enhance both the quality of the images produced and the comfort experienced by patients. By evaluating different MRI acquisition techniques, the study seeks to identify methods that can reduce discomfort and improve diagnostic outcomes. Participants will include healthy subjects and patients undergoing various MRI examinations as part of their clinical care. The study will assess the effectiveness of these optimized sequences in real-world settings.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 who require an MRI examination of specific anatomical areas as part of their clinical follow-up.
Not a fit: Patients with contraindications to MRI or those who cannot undergo the examination due to specific medical conditions will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more comfortable and higher-quality MRI examinations for patients.
How similar studies have performed: While there have been studies focusing on MRI optimization, this specific approach to enhancing comfort and quality through acquisition sequence adjustments is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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).
Where this trial is running
Nancy
- CHRU de Nancy — Nancy, France (RECRUITING)
Study contacts
- Study coordinator: Valérie LAURENT, MD, PhD
- Email: v.laurent@chru-nancy.fr
- Phone: +33383154181
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Healthy Subjects, Patient Performing an MRI Examination