NCT03452410CompletedNot Applicable
Positive Diagnosis of Vestibular Neuritis Using Fluid Attenuated Inversion Recuperation (FLAIR) Sequence, One Hour After Intravenous Gadolinium Injection, on a 1.5 Tesla
University Hospital, Strasbourg, France1 site in 1 country35 target enrollmentStarted: February 23, 2018Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 35
- Locations
- 1
- Primary Endpoint
- Diagnosis of vestibular neuritis
Study Overview
Brief Summary
Our objective is to allow positive MRI diagnosis of vestibular neuritis by highlighting contrast enhancement of the vestibular nerve on the pathological side of the FLAIR sequence acquired 1h after intravenous gadolinium injection in patients with typical vestibular neuritis. At present, the diagnosis is based on a combination clinical examination / video-head impulse test, and no imaging examination allows the diagnosis to be positive.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Age 18-80 years
- •Presence of a typical unilateral vestibular neuritis during the ENT examination with videonystagmography
- •Subject having his agreement for the use of his medical data for research purposes.
Exclusion Criteria
- •Special clinical forms of the disease: doubtful or atypical forms, especially the presence of deafness
- •Treatments and related interfering diseases, antecedents: antecedents of neuritis for controls, presence of vertigo, bilateral involvement
- •Impossibility to give the subject information enlightened (subject in emergency situation, difficulties of understanding the subject, ...)
- •Subject under the protection of justice
- •Subject under guardianship or curatorship
Outcomes
Primary Outcomes
Diagnosis of vestibular neuritis
Time Frame: one hour after intravenous gadolinium injection
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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