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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms

  • Superior Semicircular Canal Dehiscence

NCT number NCT06170398
Study type Interventional
Source University Hospital, Toulouse
Contact Yohan Gallois, Dr
Phone 05-61-77-77-04
Email gallois.y@chu-toulouse.fr
Status Not yet recruiting
Phase N/A
Start date January 2024
Completion date January 2026

See also
  Status Clinical Trial Phase
Withdrawn NCT01727544 - Vestibular Function Outcome After Cartilage Cap Occlusion Surgery Phase 0