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Clinical Trial Summary

The purpose of this study is to gather long-term data on the FDA approved CI532 cochlear implant, and CP1000 (Nucleus 7) sound processor

Clinical Trial Description

Appropriate candidates will receive a CI532 cochlear implant and be fit with the CP1000 sound processor. Imaging will be completed pre-op, intra-op, and post-op to assess implant location. Speech perception testing as well as subjective questionnaires will be administered over 12 months. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT03007472
Study type Interventional
Source Cochlear
Status Completed
Phase N/A
Start date February 15, 2017
Completion date March 6, 2020

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