Evaluation of Sound Processor for a Transcutaneous System

Status Completed

Clinical Trial Summary

A single center study evaluating the performance of an externally worn sound processor for a transcutaneous bone anchored hearing system using audiological outcomes measures such as aided thresholds and speech intelligibility and self evaluation questionnaires.

Clinical Trial Description

Bone conduction hearing systems use the body's natural ability to transfer sound through bone conduction. The sound processor picks up sound and converts it into vibrations that are transferred through the skull bone to the inner ear (cochlea). Thus, for patients with conductive or mixed hearing losses, patients with lasting hearing loss following a middle ear disease or malformations (such as microtia), the vibrations are bypassing the conductive problem in the ear canal or middle ear. Bone conduction devices currently on the market are divided into three types; transcutaneous direct drive, percutaneous (skin penetrating) direct drive and transcutaneous skin drive bone conduction devices. This evaluation focus on a sound processor used for a transcutaneous system. ;

Study Design

Related Conditions & MeSH terms

Conductive Hearing Loss
Deafness
Hearing Loss
Hearing Loss, Conductive
Hearing Loss, Mixed Conductive-Sensorineural
Mixed Hearing Loss

Clinical Trial Details

NCT number	NCT03374787
Study type	Interventional
Source	Oticon Medical
Contact
Status	Completed
Phase	N/A
Start date	November 15, 2017
Completion date	November 22, 2018

View Details

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