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Quality Control of CE-Certified Phonak Hearing Aids - 2016_05

Hearing Loss Clinical Trial

Official title:
Quality Control of CE-Certified Phonak Hearing Aids

Clinical Trial Summary

A methodical evaluation of new CE-labelled Phonak Hearing Systems is intended to be conducted on hard of hearing participants to grant quality control prior to product launch. The aim of the investigation series is to ensure zero-defect overall performance of the new hearing systems as well as maximum benefit for the participant with the devices in comparison to previously outstanding Phonak Hearing Systems.

Clinical Trial Description

Phonak Hearing Systems pass through different development and study stages. At an early stage, feasibility studies are conducted to investigate new algorithms, features and functions in an isolated manner. If the benefit is proven, their performance is then investigated regarding interdependency between all available algorithms, features and functions running in parallel in a hearing aid (pivotal/pre-validation studies) and, as a result, they get optimized. Afterwards, and prior to product launch, the Phonak Hearing Systems undergo a final quality control in terms of clinical trials in the way as planned for this study ("phase of final inspection"). This will be a controlled, single blinded and randomised active comparator clinical evaluation which will be conducted mono centric at Sonova AG Headquarters based in Stäfa (Switzerland). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02951247
Study type Interventional
Source Sonova AG
Contact
Status Completed
Phase N/A
Start date November 8, 2016
Completion date February 20, 2017
View Details
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