MedTrace Logo

Evaluation of the Baha SoundArc in Pediatric Patients

NCT03333577 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2019-04-30

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to gather clinical performance data on the Baha SoundArc

Conditions

  • Hearing Loss, Conductive
  • Hearing Loss, Mixed
  • Hearing Loss, Unilateral

Interventions

DEVICE

SoundArc

non-surgical attachment method for wearing a bone conduction hearing system

Sponsors & Collaborators

  • Cochlear

    lead INDUSTRY

Principal Investigators

  • George Cire · Study Director

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
5 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-02
Primary Completion
2018-11-02
Completion
2018-11-02
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT03333577 on ClinicalTrials.gov