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Bone Conduction Auditory Performance Via the Tooth for Single-Sided Deafness

NCT00977314 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2014-10-17

Study results available
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Summary

The purpose of this study is to determine the safety and efficacy of using bone conduction via the teeth to treat Single-Sided Deafness (SSD).

Conditions

  • Unilateral Hearing Loss

Interventions

DEVICE

The Sonitus Bone Conduction Hearing System

Comparison of HINT scores (Speech front with noise at better ear) at 30 days tested with the device in place verses with the device removed.

DEVICE

SoundBite

DEVICE

SoundBite Hearing System

Sponsors & Collaborators

  • Sonitus Medical Inc

    lead INDUSTRY

Principal Investigators

  • Michael Murray, MD

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2010-02-28
Completion
2010-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00977314 on ClinicalTrials.gov