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Evaluation of Performance and Usability of N6 in the Paediatric Population

NCT01800929 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2013-03-01

No results posted yet for this study

Summary

The purpose of this study is to evaluate the performance and usability of the N6 system in children with the N5 system.

Conditions

Interventions

DEVICE

N6

Children with N5 will be upgraded to the N6 for a period of up to 2 months to evaluate.

Sponsors & Collaborators

  • The HEARing Co-operative Research Centre, Melbourne

    collaborator UNKNOWN

  • Melbourne Cochlear Implant Clinic, Melbourne

    collaborator UNKNOWN

  • The Shepherd Centre, Sydney

    collaborator UNKNOWN

  • Hear and Say Centre

    collaborator OTHER

  • The Hearing House, Auckland

    collaborator UNKNOWN

  • Cochlear, Asia Pacific

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • Australia
  • New Zealand

Study Locations

More Related Trials

Entities

Diseases

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 NCT01800929 on ClinicalTrials.gov