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Clinical Trial Summary

The purpose of this feasibility study is to evaluate whether low-frequency acoustic hearing sensitivity can be preserved in newly implanted adults with partial deafness (considerable low frequency acoustic hearing profiles with severe-to-profound high frequency sensorineural hearing loss) using the HiResolution™ 90K™ Advantage cochlear implant with the HiFocus™ Mid-Scala electrode to support the development of electro-acoustic stimulation technology (EAS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02189798
Study type Interventional
Source Advanced Bionics
Contact
Status Terminated
Phase N/A
Start date October 21, 2014
Completion date March 29, 2022

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