Optimization of the Acquisition Sequence to Improve the Quality and Comfort of Magnetic Resonance Imaging Exam

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

720 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-04

Study Completion Date

2028-12-01

Brief Summary

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The purpose of this study is to evaluate the optimization of MRI acquisition sequences.

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Detailed Description

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Conditions

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Healthy Subjects Patient Performing an MRI Examination

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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All subjects will have an MRI examination

Group Type EXPERIMENTAL

MRI examination

Intervention Type OTHER

All subjects (healthy subjects and patients) will have an MRI examination with optimized sequences

Interventions

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MRI examination

All subjects (healthy subjects and patients) will have an MRI examination with optimized sequences

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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.

* 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

* any contraindication to MR examination (active medical device, ferromagnetic foreign body, pregnancy, morbid obesity, claustrophobia, … ),
* subject under a measure of legal protection.

* 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.

* to have a limited MRI examination time due to a sensitive clinical situation (sedation, unstable hemodynamic state, postoperative).

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes