At a glance
ClinicalIndex Comparison RecordN/ACompleted· 35 enrolled
Drug / intervention
The Sonitus Bone Conduction Hearing System +2 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Bone Conduction Auditory Performance Via the Tooth for Single-Sided Deafness
In Brief
A clinical study evaluating The Sonitus Bone Conduction Hearing System, SoundBite, and 1 other intervention for Unilateral Hearing Loss. Completed, enrolled 35 participants across 2 sites.
Detailed 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).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsUnilateral Hearing Loss
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartSep 2009
First PostedSep 2009
Primary CompletionFeb 2010
TodayJul 2026
First PostedSep 15, 2009
Enrollment StartSep 1, 2009
Primary CompletionFeb 1, 2010
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 16.8 years ago
Interventions
The Sonitus Bone Conduction Hearing Systemdevice
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.
SoundBitedevice
SoundBite Hearing Systemdevice