Status:

COMPLETED

Quality of Life With Bone Conduction Hearing Device

Lead Sponsor:

Medical University of Vienna

Conditions:

Conductive Hearing Loss

Eligibility:

All Genders

13+ years

Phase:

NA

Brief Summary

The aim of this study is to compare the audiological and quality of life performance patients have with an ADHEAR (adhesive bone conduction device) compared to no hearing device.

Detailed Description

Patients will be recruited at the outpatient's department of the Medical University of Vienna - Otorhinolaryngology department. Patient will be asked to participate in the study when inclusion and exc...

Eligibility Criteria

Inclusion

  • Unilateral and/or bilateral conductive hearing loss (CHL)
  • Conductive hearing loss \>10 decibel on average
  • Subjective benefit from the device
  • Subjects aged 13 years or older
  • Capable of the German language
  • Willingness and ability to perform all tests required for the study
  • Signed, and dated informed consent before the start of any study specific procedure

Exclusion

  • Pregnancy or breastfeeding
  • Patient uses a hearing aid or plans to acquire a hearing aid
  • Patient is intolerant of the materials as described by Manufacturer
  • Patient presents with a skin or scalp condition that may preclude the attachment of the adhesive adapter.
  • Patient cannot perform the audiological tests or is unable to fill out the questionnaires.
  • Patient presents with retrocochlear, or central auditory disorder.
  • any physical, psychological, or emotional disorder that would interfere with the ability to perform on test and rehabilitation procedures

Key Trial Info

Start Date :

February 25 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 31 2024

Estimated Enrollment :

24 Patients enrolled

Trial Details

Trial ID

NCT03864731

Start Date

February 25 2019

End Date

October 31 2024

Last Update

May 13 2025

Active Locations (1)

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MUW AKH

Vienna, Austria, 1090