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When patients arrive in the waiting room of the MRI department, patients will be given the briefing note explaining the purpose of the study and how it is going. During the consultation, the radiologist will check the inclusion and non-inclusion criteria, and will take the time to answer all of the patient's questions about the study (or his family member by telephone if the patient does not is not in a condition to give its consent). The MRI examination will be performed on a 3T multi-parametric MRI. If the neurological disorder presented by the patient does not require an injection as part of routine care, only a high resolution 3D T2 sequence on the nasosinus cavities and the olfactory tract, called bFFE-Xd for approximately 2 min. If the neurological disorder presented by the patient requires an injection as part of current care, the examination will be completed with the nasosinus and olfactory 3D bFFE-Xd sequence, and the following additional sequences performed after post injection: a * 3D FABIR 0.9 sequence covering the brain, dedicated to exploring the subarachnoid spaces; * a 3D T1 TSE 0.7 sequence covering the brain looking for meningeal or encephalic contrast enhancement, * FLAIR HR coronal sequence (high resolution) exploring the limbic system. * Optional: a 3D FLAIR "labyrinth" sequence in the event of hearing / balance problems; a DCE infusion sequence (T1-WI) on the olfactory tract if olfactory disorder, which will be the first sequence made at the time of injection.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Fondation A De Rothschild
Paris, France
Start Date
May 20, 2020
Primary Completion Date
December 19, 2023
Completion Date
December 19, 2023
Last Updated
December 20, 2023
100
ACTUAL participants
MRI
OTHER
Lead Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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