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MRI Exploration of Meningeal Inflammatory Disease (EIME)

F

Fondation Ophtalmologique Adolphe de Rothschild

Status

Completed

Conditions

MRI

Treatments

Device: MRI with gadolinium injection

Study type

Observational

Funder types

NETWORK

Identifiers

NCT04707170
JSY_2020_38

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 two additional sequences of 6 minutes duration will be added.

The MRI of routine care includes at least the following sequences:

  • 3D T1 TFE 1.0 isotropic (2 minutes)
  • T2 TSE (2 minutes)
  • 3D FLAIR pre-injection (opt) (3 minutes)
  • 3D FLAIR post-injection (3 minutes)

As part of the research, the following sequences will be acquired:

  • FABIR pre-injection (3 minutes)
  • FABIR post-injection (3 minutes)

Patients hospitalized for a foreseeable duration of at least 24 hours will be offered participation in the longitudinal tab of the study, for which four non-injected MRI examinations will be performed. The examinations will be carried out remotely from the injected MRI (1h, 2h, 12h-15h, 24h-36h). These exams dedicated to research will include the following sequences for a maximum of 8 minutes:

  • 3D T1 TFE 1.0 isotropic (2 minutes)
  • 3D FLAIR (3 minutes)
  • FABIR (3 minutes)

Enrollment

302 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient over 18 years old
  • To benefit as part of his treatment of an MRI with injection of gadolinium
  • Express consent to participate in the study
  • Affiliate or beneficiary of a social security scheme

For the ancillary study to meet secondary endpoint number 5:

  • Patient over 18 years old
  • To benefit as part of his treatment of an MRI with injection of gadolinium
  • Hospitalized for an expected period of at least 48 hours after the time of inclusion
  • 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

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Central trial contact

amélie YAVCHITZ; julien savatovsky

Data sourced from clinicaltrials.gov

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