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Clinical Performance of a Transcutaneous Bone Conduction Hearing Solution (Baha® Attract System)

Hearing Loss Clinical Trial

Official title:
Clinical Performance of a Transcutaneous Bone Conduction Hearing Solution (Baha® Attract System). A Multicentre, Open, Prospective Clinical Investigation. 3 Months Investigation With a 6 Months Follow-up

Clinical Trial Summary

The rationale behind this clinical performance investigation is to collect data regarding the usability of the Baha Attract System in patients with hearing impairment that are candidates for Baha surgery:

- To describe the expected hearing performance with the Baha Attract in comparison to unaided hearing thresholds or a pre-test situation using a sound processor together with a softband

- Which sound processor to select, i.e. BP100 vs BP110

- Improve the fitting process for the sound processor

- Selection of sound processor magnet at time of fitting and over time

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01822119
Study type Interventional
Source Cochlear Bone Anchored Solutions
Contact
Status Completed
Phase N/A
Start date March 2013
Completion date February 2014
View Details
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