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Clinical Trial Summary

This study aims to evaluate the safety and efficacy of cochlear implantation for adults with bilateral sensorineural hearing loss who currently do not meet the FDA-approved indications for cochlear implantation. Following cochlear implantation, participants will complete speech perception assessments and questionnaires over the course of seven visits.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06293482
Study type Interventional
Source Cochlear
Contact Lavin Entwisle
Phone 605-354-2917
Email lentwisle@cochlear.com
Status Not yet recruiting
Phase N/A
Start date July 2024
Completion date June 2028

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