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Early Experience of a New Implant System for Bone Conduction Hearing in the Pediatric Population

NCT03509974 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2021-10-22

Study results available
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Summary

To study the initial experience with implanting and fitting a new Bone Conduction system in pediatric patient population with conductive, mixed or single-sided deafness.

Conditions

  • Unilateral Mixed Conductive and Sensorineural Hearing Loss (Diagnosis)
  • Sensorineural Hearing Loss, Unilateral With Normal Hearing on the Contralateral Side

Interventions

DEVICE

Osseointegrated Steady State Implant

Bone anchored, bone conduction hearing system

Sponsors & Collaborators

  • Cochlear

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
5 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-18
Primary Completion
2020-02-20
Completion
2020-03-19

Countries

  • Canada

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 NCT03509974 on ClinicalTrials.gov