Study of Multifrequential Impedancemetry in Pulsatile Tinnitus
NCT ID: NCT06290999
Last Updated: 2025-02-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
50 participants
OBSERVATIONAL
2024-06-03
2026-03-15
Brief Summary
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Detailed Description
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Investigators will include every patient that consult to Ear, Nose and Throat unit of Bordeaux University Hospital with a pulsatile tinnitus trouble, and perform multifrequential admittancemetry. If a radio-surgical intervention is scheduled for a venous stenosis, the test will also be performed test after the surgery.
If there is no surgical intervention, no follow-up will be required.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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patient with pulsatile tinnitus
multifrequential admittancemetry
Every participant of the study have to complete an Ear, Nose and Throat examination included a conventional audiometry, and a multifrequential admittancemetry.
if radio-interventional venous stenting is not indicated, an multifrequential admittancemetry will also be performed 3 months after the procedure.
Interventions
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multifrequential admittancemetry
Every participant of the study have to complete an Ear, Nose and Throat examination included a conventional audiometry, and a multifrequential admittancemetry.
if radio-interventional venous stenting is not indicated, an multifrequential admittancemetry will also be performed 3 months after the procedure.
Eligibility Criteria
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Inclusion Criteria
* Unilateral or bilateral pulsatile tinnitus
* Pulsatile tinnitus \> 1 month old
* Affiliated or beneficiary of by social security system
Exclusion Criteria
* Middle ear abnormality (any type of partial or total filling of the middle ear) noted on otoscopy or subsequent MRI scan
* Abnormal eardrums excluding tympanosclerosis
* Non-pulsatile tinnitus
* Conductive hearing loss with abolition of stapedial reflexes
* Minor patient
* Major protected
* Abnormal tympanometry at 226 Hz
* Presence of rotatory vertigo
* Opposition to participation expressed by patient
18 Years
ALL
No
Sponsors
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University Hospital, Bordeaux
OTHER
Responsible Party
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Locations
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Bordeaux University Hospital
Bordeaux, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CHUBX 2023/80
Identifier Type: -
Identifier Source: org_study_id
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