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临床试验/NCT00451503
NCT00451503已完成不适用

Evaluation of Middle Ear Implants in the Therapeutic Strategy of Auditory Rehabilitation in Case of Failure of Conventional Hearing Aid

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 69 人开始时间: 2007年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
69
试验地点
2
主要终点
Assessment of the middle ear implant on speech intelligibility in quiet and noise in case of failure of conventional hearing aid

研究概览

简要总结

The middle ear implant are used for patients with mild to severe sensorineural hearing loss, who cannot benefit from conventional hearing aids because of medical reasons such as chronic external otitis or external skin irritation. The device is also available for patients who are dissatisfied with the conventional hearing aids because of poor sound quality, feedback or occlusion of the ear canal. To date, more than 1500 patients have been implanted in Europe and about more than 600 patients in France. The aim of the present study is to compare in a randomized study the performances of the system to those of the conventional hearing aid in patients with similar degree of hearing loss.

详细描述

Objective

The main objective of this study is to demonstrate that the middle ear implant increases the hearing in terms of speech intelligibility in quiet and noisy conditions, in patients who have no further benefit of their conventional hearing aid. The quality of life of these patients will be evaluated as well as the tolerance of the middle ear implant after 6 months.

Design of the study: 420 patients with mid or severe hearing loss will be included. They will have for 3 months the best conventional hearing aid adapted to their hearing loss. The first 84 patients who will not have a benefit of this hearing aid, will be randomised in two groups. The patients of the first group will be operated as soon as possible, the surgery of the patients of the second group will be delayed by 6 months. The whole duration of the study is 48 months.

Evaluation criteria: Audiological testing (pure-tone hearing thresholds, speech comprehension in quiet and noise), and subjective evaluation using self-assessment scales will be performed before and 6 months after the implantation in the two groups.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adults patients
  • hearing loss
  • accept to participate
  • having health insurance

排除标准

  • known disease that needs MRI follow up
  • contraindication to middle ear surgery

结局指标

主要结局

Assessment of the middle ear implant on speech intelligibility in quiet and noise in case of failure of conventional hearing aid

时间窗: during the study

次要结局

  • Assessment of the tolerance at 6 months postoperative of the middle ear(6 months postoperative)
  • Assessment of the life quality of patients(during the study)
  • implantation(during the study)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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