Outcomes in Adults With Mixed or Conductive Hearing Loss Implanted With the BONEBRIDGE

Status: Terminated
Location: See all (3) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults, 18 years of age or older at the time of implantation

• Conductive or mixed hearing loss, defined as:

• Conductive hearing loss with pure-tone average (PTA) for bone conduction thresholds better than or equal to 25 dB at 500, 1000, 2000 and 3000 Hz

• Mixed hearing loss with PTA for bone conduction thresholds better than or equal to 45dB at 500, 1000, 2000, and 3000 Hz

• Air-bone gap greater than or equal to 30 dB at 500, 1000, 2000, and 3000 Hz

• Ability to benefit from amplification as defined by a monosyllabic (CNC) word score of 30% correct or better

• Bilateral BONEBRIDGE can be considered if the difference in PTA for bone conduction thresholds is 10 dB or less between the right and left ears

• Prior experience with acoustic or bone conduction hearing aids, unless candidate is unable to wear amplification for medical reasons

• Able to complete testing materials in English

• CT scan indicating the patient's anatomy is adequate to enable placement of the implant

• Ability to undergo general anesthesia

• Appropriate motivation and expectation levels

• Stated willingness to comply with all study procedures for the duration of the study

Locations
United States
Ohio
The Ohio State Wexner Medical Center University
Columbus
Pennsylvania
The Hospital of the University of Pennsylvania
Philadelphia
Other Locations
Canada
London Health Sciences Centre
London
Time Frame
Start Date: 2019-08-26
Completion Date: 2022-11-04
Participants
Target number of participants: 9
Treatments
Experimental: Bone Conduction Implant
All subjects will be implanted with the bone conduction implant.
Authors
Related Therapeutic Areas
Sponsors
Leads: Med-El Corporation

This content was sourced from clinicaltrials.gov