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

C

Central Hospital, Nancy, France

Status

Enrolling

Conditions

Healthy Subjects
Patient Performing an MRI Examination

Treatments

Other: MRI examination

Study type

Interventional

Funder types

Other

Identifiers

NCT04645628
2020-A01969-30

Details and patient eligibility

About

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

Enrollment

720 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and 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).

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

720 participants in 1 patient group

All subjects will have an MRI examination
Experimental group
Treatment:
Other: MRI examination

Trial contacts and locations

1

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Central trial contact

Valérie LAURENT, MD, PhD; Gabriela HOSSU, PhD

Data sourced from clinicaltrials.gov

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