跳至主要内容
临床试验/ACTRN12610000773033
ACTRN12610000773033尚未招募未知

Prescription Procedures for Cochlear Hybrid Devices to optimise the acoustic-to electric output requirements for adults who use a Hybrid device.

The HEARing Cooperative Research Centre Limited0 个研究点目标入组 16 人开始时间: 2010年9月16日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • 1. Will be eighteen years of age or older at the time of evaluation.
  • 2. Will be users of a Cochlear Hybrid System with a minimum of 12 months experience prior to enrolment.
  • 3. The audiometric criteria for residual hearing in the implanted ear will be within the range of normal to profound.
  • 4. A willingness to wear all device conditions (New hearing aids and Hybrid sound processor) on a daily basis for the duration of the study.
  • 5. A willingness to participate in and to comply with all requirements of the protocol including a willingness to complete all tests and questionnaires.

排除标准

  • 1. Children under the age of 18 years of age.
  • 2. People whose primary language is other than English (LOTEs).
  • 3. Additional needs or disability that would prevent participation in evaluations.
  • 4. Unrealistic expectations on the part of the participant, regarding the possible benefits and limitations of the study.

研究者

发起方
The HEARing Cooperative Research Centre Limited

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