NCT05326581

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
750

participants targeted

Target at P75+ for all trials

Timeline
11mo left

Started May 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress82%
May 2022May 2027

First Submitted

Initial submission to the registry

March 18, 2022

Completed
26 days until next milestone

First Posted

Study publicly available on registry

April 13, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

May 23, 2022

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2027

Last Updated

January 5, 2026

Status Verified

December 1, 2025

Enrollment Period

4.9 years

First QC Date

March 18, 2022

Last Update Submit

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

Device: mri

VOLUNTEERS

healthy volunteers among staff.

Device: mri

Interventions

mriDEVICE

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.

PATIENTSVOLUNTEERS

Eligibility Criteria

Age18 Months+
Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Interventions

Magnetic Resonance Imaging

Intervention Hierarchy (Ancestors)

TomographyDiagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Study Officials

  • Julien Savatovksy, MD

    Fondation A. de Rothschild

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Amélie Yavchitz, MD

CONTACT

Julien Savatovsky, MD

CONTACT

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

Locations