Long Term Safety of the Sonitus SoundBite System

NCT01108406 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2014-10-20

Study results available
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Summary

The objective of this study is to assess the long-term safety and quality of life improvement of the Sonitus SoundBite Hearing System.

Conditions

  • Hearing Loss
  • Unilateral Hearing Loss
  • Total Unilateral Deafness

Interventions

DEVICE

Sonitus SoundBite System

Non Surgical Bone Conduction Device

DEVICE

SoundBite Hearing System

Sponsors & Collaborators

  • Sonitus Medical Inc

    lead INDUSTRY

Principal Investigators

  • Michael Murray, MD · Camino ENT

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
2010-04-30
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • United States

Study Locations

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Entities

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 NCT01108406 on ClinicalTrials.gov