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MR7T-Healthy-PTX : Brain Exploration in Magnetic Resonance Imaging in Parallel Transmission Mode (pTX) at 7 Tesla

P

Poitiers University Hospital

Status

Unknown

Conditions

MRI
PTX
BRAIN
7 TESLA

Treatments

Other: MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT04369755
2019-A02689-48

Details and patient eligibility

About

Magnetic resonance imaging (MRI) is a non-invasive imaging modality used in routine clinical practice for clinical diagnosis by visualizing the anatomical structure and in vivo function of certain organs. The development of ultra-high field MRI systems with 7.0-T or higher, gives access to a new field of exploration of the human body by improving the speed of acquisition but also a better signal-to-noise ratio (SNR) and better resolution. In order to fully exploit the potential of these ultra-high field MRI scanners, various technical issues must be adressed. Indeed, the non-uniformity of the transmission field is one of them leading to non-uniform images with spatially varying contrast. Thus the pTX (parallel transmission) mode using multiple transmission channels allows spatial and temporal control over the RF waves.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years old
  • Subject with no MRI contraindications (metallic shine, pacemaker)
  • Free subject, without guardianship or curatorship or subordination
  • A person affiliated to or beneficiary of a social security scheme.
  • Informed and signed consent by the healthy volunteer after clear and fair information about the study

Exclusion criteria

  • Subject with a contraindication to MRI (pregnancy, ocular metallic foreign body (accidental or other shrapnel); pacemaker (cardiac stimulator), implantable defibrillator, non MRI 7.0 T compatible neurostimulator, cochlear implants and generally any irremovably implanted electronic medical device; metallic heart valve, vascular clips formerly implanted on cranial aneurysm), metallic prostheses.
  • Healthy volunteers suffering from claustrophobia
  • Persons not benefiting from a Social Security scheme or not benefiting from it through a third party.
  • Persons benefiting from reinforced protection, i.e. minors, pregnant and breastfeeding women, persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social institution, adults under legal protection and finally, patients in emergency situations.
  • Pregnant or breastfeeding women, women of childbearing age who do not have effective contraception (hormonal/mechanical: per os, injectable, transcutaneous, implantable, intrauterine device, or surgical: tubal ligation, hysterectomy, total oophorectomy).

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

MRI
Other group
Description:
A MRI on PTX mode will be done on healthy subjects (approx. 90 min of sequences)
Treatment:
Other: MRI

Trial contacts and locations

1

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Central trial contact

Rémy GUILLEVIN, Pr

Data sourced from clinicaltrials.gov

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