ClinicalTrials.Veeva

Menu

Comparison of the Performance of an Optimized 3D EPI SWI Sequence and a Non-EPI QSM SWI Sequence in Detecting the Central Vein Sign in Patients With Multiple Sclerosis (COPEQ-MS)

F

Fondation Ophtalmologique Adolphe de Rothschild

Status

Active, not recruiting

Conditions

Multiple Sclerosis

Treatments

Device: cerebral MRI

Study type

Observational

Funder types

NETWORK

Identifiers

NCT04705870
JSY_2020_39

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 four additional 20-minute sequences will be added.

MRI of routine care in the context of MS includes at least the following sequences:

  • 3D T1 TFE (2 minutes)
  • T2 TSE (2 minutes)
  • 3D FLAIR (3 minutes)
  • SWI EPI 0.6 iso (7 minutes)

The sequences added by the search are:

  • SWI non EPI QSM 6 echo (10 minutes)
  • SWI EPI in resolution equivalent to non-EPI SWI (3 minutes)
  • SWI EPI to TR equivalent to SWI non EPI (6 minutes)

These sequences will be acquired before or after the injection of gadolinium (if present in the examination of routine care). For examinations carried out with injection, the order of carrying out the 4 post-injection SWI sequences will be random.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients over 18
  • With MS defined according to the McDonald's revised clinical or radiological spatial and temporal dissemination criteria, with onset of symptoms <5 years
  • To benefit as part of care from an MRI with or without injection of gadolinium
  • Express consent to participate in the study
  • Affiliate or beneficiary of a social security scheme

Exclusion criteria

  • Patient benefiting from a legal protection measure
  • Pregnant or breastfeeding woman

Trial contacts and locations

1

Loading...

Central trial contact

amélie YAVCHITZ; julien savatovsky

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems