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Electro-physiological Findings and Symptoms Severity in Superior Canal Dehiscence

Interest of Electro-physiological Findings in the Assessment of Symptoms Severity in Superior Semi-circular Canal Dehiscence Syndrome

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06170398
Acronym
INTEX-DEHI
Enrollment
115
Registered
2023-12-14
Start date
2024-01-31
Completion date
2026-01-31
Last updated
2023-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Superior Semicircular Canal Dehiscence

Keywords

Superior semi-circular canal dehiscence, Minor syndrome, Pulsatile tinnitus, Autophony Tullio phenomenon

Brief summary

This research aims at assessing the validity of three different electro-physiological tests (Vestibular Evoked Myogenic Potentials, WideBand Tympanometry, Electrocochleography) used in the investigation of the symptoms severity in the case of superior semi-circular canal dehiscence syndrome.

Detailed description

Superior semi-circular canal dehiscence (SCD) syndrome can associate several cochlear and vestibular symptoms. Recent systematic reviews identified pulsatile tinnitus, autophony, sound-induced and pressure-induced vertigo as most specific signs of SCD. These signs are rarely all present and the symptomatology remains highly variable from a patient to another, with frequent though less evocative symptoms such as dizziness or ear pressure. A surgical treatment may be proposed when the symptoms become significantly incapacitating. Unfortunately to date, there is no objective marker of this severity and all surgical decisions rely on the importance of patients' complaints. High Resolution Computed Tomography (HRCT) of the temporal bone can confirm the diagnosis. Electro-physiological investigations such as Vestibular Evoked Myogenic potentials (VEMPs) have also been extensively described in the diagnosis of SCD but they have been reported as independent from the symptoms severity. Wideband tympanometry (WBT) and Electrocochleography (EcoG) have only been studied in few reports but the latter appears as a promising tool in the assessment of the symptoms because it explores inner ear biomechanics, directly involved in the pathophysiology of this condition.

Interventions

DIAGNOSTIC_TESTWideband tympanometry

Wideband tympanometry

DIAGNOSTIC_TESTElectrocochleography

Electrocochleography

Vestibular Evoked Myogenic potentials

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* confirmed unilateral SCD (using specific HRCT settings and reconstructions) with or without SCD symptoms * if present, SCD symptoms should be stable * patients understanding and reading french * affiliated to social security.

Exclusion criteria

* bilateral confirmed SCD * doubtful SCD * other otologic or neurotologic condition that might mimick SCD symptomatology : middle ear conditions, Meniere disease, vestibular migraine

Design outcomes

Primary

MeasureTime frameDescription
EcoG validity - pulsatile tinnitus30 daythe validity of EcoG will be assessed by the correlation between the alteration of the summating potential/action potential ratio and symptom severity (pulsatile tinnitus) assessed by a visual analogue scale (0 to 10)
EcoG validity - autophony30 daythe validity of EcoG will be assessed by the correlation between the alteration of the summating potential/action potential ratio and symptom severity (autophony) assessed by a visual analogue scale (0 to 10)
EcoG validity - dizziness induced by loud sounds30 daythe validity of EcoG will be assessed by the correlation between the alteration of the summating potential/action potential ratio and symptom severity (dizziness induced by loud sounds) assessed by a visual analogue scale (0 to 10)
EcoG validity - dizziness induced by pressure changes30 daythe validity of EcoG will be assessed by the correlation between the alteration of the summating potential/action potential ratio and symptom severity (dizziness induced by pressure changes) assessed by a visual analogue scale (0 to 10)

Countries

France

Contacts

Primary ContactYohan Gallois, Dr
gallois.y@chu-toulouse.fr05-61-77-77-04
Backup ContactMathieu MARX, Pr
marx.m@chu-toulouse.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026