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Clinical Trial Summary

Approximately thirty subjects with mixed or conductive hearing loss, meeting FDA-cleared candidacy criteria for the BONEBRIDGE, will be implanted and followed for three (3) months post-activation to assess safety and effectiveness of the BONEBRIDGE implant.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03859648
Study type Interventional
Source Med-El Corporation
Contact
Status Terminated
Phase N/A
Start date August 26, 2019
Completion date November 4, 2022

See also
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