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RECRUITING
NCT05300698

MRI Versus Ocular UltraSonography for a Non Contact Evaluation of Ocular Layers

Sponsor: Fondation Ophtalmologique Adolphe de Rothschild

View on ClinicalTrials.gov

Summary

D0: inclusion visit * information * Realization of the ocular ultrasound (care) * Collection of consent * Realization of high resolution MRI with injection of contrast product (duration of 30 minutes) For the realization of the MRI, the contrast product used is the gadobutrol. The dose, the lowest allowing an enhancement of sufficient contrast for diagnostic purposes (0.1 mmol/kg body mass body), is administered as a bolus intravenously in the lying patient. The MRI examination can begin immediately after injection. The patient should be monitored for at least half an hour after this, the majority of undesirable effects occurring at the during this period. The indication of ocular ultrasound and ophthalmological follow-up of the patient up to 1 month after inclusion will be collected at from their medical records.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

30

Start Date

2024-01-23

Completion Date

2026-11

Last Updated

2026-01-05

Healthy Volunteers

No

Interventions

DEVICE

MRI

compare between MRI and ultrasound for indirect assessment of ocular layers

Locations (1)

Hopital Fondation Adolphe de Rothschild

Paris, Paris, France