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Development, Implementation and Initiation of Normative Database Quantitative Ultra High Field MRI Paramaters

P

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Unknown

Conditions

Healthy

Treatments

Procedure: acquisition of normative database with ultra high field MRI
Device: MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT02402751
2015-A0012148

Details and patient eligibility

About

The Centre for Magnetic Resonance in Biology and Medicine (CRMBM, UMR-CNRS 7339 AMU) obtained funding for a whole body NMR imaging at 7. It is the only MRI at 7T installed in a hospital in France (only two 7T MRI in France) and therefore a unique opportunity to develop new diagnostic approaches.

The purpose of this study is to develop, implement and validate new MRI quantitative parameters derived from ultra high field MRI in order to characterize non-invasively with an unprecedented resolution and sensitivity, anatomy as well as certain physiological, hemodynamic and metabolic function of brain, spinal cord, musculoskeletal system, and heart in healthy subjects

Full description

The key is that the goal of our projects is not only producing images of better quality than using a 3T scanner but also making images differently, by highlighting new contrasts and features of theses organs in order to improve the diagnosis and prognosis of neurological, psychiatric, cardiovascular and rheumatologic diseases.

Enrollment

400 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • People not presenting contraindications to the MRI (pacemaker, agitation, metallic brightness, claustrophobia etc.)
  • People having no intra-physical object potentially conductive.
  • People having no affection after detailed interrogation

Exclusion criteria

  • People staying in a sanitary or social establishment
  • People in emergency situation
  • People not wishing to be informed about anomalies in the MRI
  • Pregnancy

Trial design

400 participants in 1 patient group

Acquisition of normative database
Experimental group
Description:
Development, implementation and initiation of normative database (image and data) quantitative ultra high field MRI paramaters
Treatment:
Procedure: acquisition of normative database with ultra high field MRI
Device: MRI

Trial contacts and locations

1

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Central trial contact

Alexandra GIULIANI; Maxime GUYE, M.D

Data sourced from clinicaltrials.gov

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