Optimization of Sequences to Improve the Quality and Comfort of the Magnetic Resonance Imaging Examination
OPTIM
1 other identifier
observational
750
1 country
1
Brief Summary
The people included will carry out an MRI comprising the sequence currently used in routine care and the different variants of the sequence being tested, for the optimization of the parameters. The duration of the examination (or the extension of the examination planned as part of patient care) will be from a few minutes to an hour depending on the sequences to be optimized. Subjects who agree to research for more than 30 minutes in the MRI machine will be compensated with a multi-brand gift voucher worth 30 euros.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2022
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 18, 2022
CompletedFirst Posted
Study publicly available on registry
April 13, 2022
CompletedStudy Start
First participant enrolled
May 23, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2027
January 5, 2026
December 1, 2025
4.9 years
March 18, 2022
December 30, 2025
Conditions
Outcome Measures
Primary Outcomes (3)
Quality of imagery
Quality of imagery evaluated on a likert-type scale (range from : "very bad quality" to "very good quality") by two experts
Baseline
Presence or absence of radiological image artifact
Presence/absence of radiological image artifact evaluated on a likert-type scale (range from : "major - impossible interpretation" to "none") by two experts
Baseline
Confidence in diagnosis
Confidence in diagnosis evaluated on a likert-type scale (range from : "not confident" to "very confident") by two experts
Baseline
Study Arms (2)
PATIENTS
patients benefiting from an MRI examination as part of their care
VOLUNTEERS
healthy volunteers among staff.
Interventions
The people included will carry out an MRI comprising the sequence currently used in routine care and the different variants of the sequence being tested, for the optimization of the parameters. The duration of the examination (or the extension of the examination planned as part of patient care) will be from a few minutes to an hour depending on the sequences to be optimized. Subjects who agree to research for more than 30 minutes in the MRI machine will be compensated with a multi-brand gift voucher worth 30 euros.
Eligibility Criteria
Participation in the study will be offered to patients performing MRI imaging as part of the treatment as well as to healthy volunteers among the staff.
You may qualify if:
- Subject over 18 years old
- Consent to participate in the study
- Member of or beneficiary of a social security scheme
- For patients: benefiting from an MRI examination as part of their care
- For volunteers: Consent to be informed if an unexpected anomaly is revealed by the imaging.
You may not qualify if:
- Subject benefiting from a measure of legal protection
- Pregnant or breastfeeding women
- For volunteers: Contraindication to MRI (detailed contraindications questionnaire, THI score \>28 questionnaire, hearing sensitivity questionnaire grade \>1)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hôpital Fondation Adolphe de Rothschild
Paris, Paris, 75019, France
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Julien Savatovksy, MD
Fondation A. de Rothschild
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NETWORK
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 18, 2022
First Posted
April 13, 2022
Study Start
May 23, 2022
Primary Completion (Estimated)
May 1, 2027
Study Completion (Estimated)
May 1, 2027
Last Updated
January 5, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share