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Évaluation de l'Impact du Compressed Sensing Sur le Signal QSM (CS-QSM)

F

Fondation Ophtalmologique Adolphe de Rothschild

Status

Completed

Conditions

MRI

Treatments

Device: MRI

Study type

Observational

Funder types

NETWORK

Identifiers

NCT04907487
JSY_2021_13

Details and patient eligibility

About

Patients who have agreed to participate in the study will complete the MRI protocol as part of routine care, to which a maximum of four additional 25-minute sequences will be added.

MRI of routine care includes at least the following sequences:

  • 3D T1 TFE (2 minutes)
  • T2 TSE (2 minutes)
  • 3D FLAIR (3 minutes)

The sequences added by the research lasting 25 minutes are:

  • SWI QSM 1.0iso 8 echoes (10 minutes)
  • SWI QSM 1.0iso 8 echoes CS 6 (7 minutes)
  • SWI QSM 1.0iso 8 echoes CS 9 (5 minutes)
  • SWI QSM 1.0iso 8 echoes CS 12 (3 minutes)

Full description

Patients who have agreed to participate in the study will complete the MRI protocol as part of routine care, to which a maximum of four additional 25-minute sequences will be added.

MRI of routine care includes at least the following sequences:

  • 3D T1 TFE (2 minutes)
  • T2 TSE (2 minutes)
  • 3D FLAIR (3 minutes)

The sequences added by the research lasting 25 minutes are:

  • SWI QSM 1.0iso 8 echoes (10 minutes)
  • SWI QSM 1.0iso 8 echoes CS 6 (7 minutes)
  • SWI QSM 1.0iso 8 echoes CS 9 (5 minutes)
  • SWI QSM 1.0iso 8 echoes CS 12 (3 minutes)

Enrollment

82 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For patients with MS:

  • Patient over 18 years old
  • Presenting MS defined according to McDonald's revised criteria for spatial and temporal clinical or radiological dissemination [16],
  • Should benefit as part of the care of an MRI examination with or without injection of gadolinium
  • Express consent to participate in the study
  • Affiliate or beneficiary of a social security scheme

For patients with an indication to undergo a brain MRI and at low risk of inflammatory CNS disease:

  • Patient over 18 years old
  • Should benefit as part of the care of an MRI examination with or without injection of gadolinium
  • Express consent to participate in the study
  • Affiliate or beneficiary of a social security scheme

Exclusion criteria

  • For patients with MS:
  • Patient benefiting from a legal protection measure
  • Pregnant or breastfeeding woman

For patients with an indication to undergo a brain MRI and at low risk of inflammatory CNS disease:

  • Patient benefiting from a legal protection measure
  • Pregnant or breastfeeding woman
  • Patient with inflammatory and / or demyelinating pathology of the CNS

Secondary exclusion criteria :

  • Motion artefact not allowing interpretation of images
  • Patient who did not perform one of the following sequences: 3D T1 TFE, 3D FLAIR (for MS patients), SWI QSM 1.0iso 8 echoes.

Secondarily excluded patients will be replaced.

Trial design

82 participants in 2 patient groups

SEP
Description:
With Multiple Sclerosis as defined by McDonald's revised clinical or radiological spatial and temporal dissemination criteria
Treatment:
Device: MRI
NO SEP
Description:
For patients with an indication to undergo a brain MRI and at low risk of inflammatory CNS disease
Treatment:
Device: MRI

Trial contacts and locations

1

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Central trial contact

amélie YAVCHITZ

Data sourced from clinicaltrials.gov

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