Hearing Loss Clinical Trial
Official title:
A Clinical Investigation of the Benefit of Directionality as a Function of Microphone Location: BTE Hearing Aids Versus ITE Hearing Aids
The current study will evaluate a new in-the-ear (ITE) hearing aid hardware. The goal is to evaluate the audiological performance, usability, feature function, and to identify unexpected or unwanted behaviour from the devices. The study plans to compare the behind-the-ear (BTE) hardware style with the ITE devices regarding the benefit received from different microphone locations.
Hearing aids constantly undergo incremental improvements from already marketed devices. The
new devices are expected to perform as well or better than the previous ITE devices.
The aim of the testing is to grant quality control prior to product launch according to
Bernafon development requirements.
The current study will evaluate a new ITE hearing aid hardware. The firmware driving the
hearing aid has already been sold on the market using the BTE hardware for almost one year
and will now be launched using the ITE custom hardware. The goal is to evaluate the
audiological performance, usability, feature function, and to identify unexpected or unwanted
behaviour from the devices. The study plans to compare the two hardware styles regarding the
benefit received from different microphone locations.
As human subjects are involved the validation falls under the definition of a clinical
investigation. The validation will address the performance of the new chip using the ITE
hardware, and ensure that there is no reduction in speech understanding between using the BTE
and ITE hardware styles. Evaluating the overall performance of the Mermaid 9 ITE devices is
important to validate that the end user is satisfied with the devices and that all user
requirements are fulfilled. All features available in Mermaid 9 have been validated and are
currently used on the market in Mermaid 9 BTE devices.
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