BONEBRIDGE Bone Conduction Implant in Adults

Status Terminated

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

Deafness
Hearing Loss
Hearing Loss, Conductive
Hearing Loss, Mixed
Hearing Loss, Mixed Conductive-Sensorineural

Clinical Trial Details

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

View Details

See also
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