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临床试验/NCT07789665
NCT07789665招募中不适用

Scientific Assessment of Auditory Intranerve Stimulation Loudness and Pitch Percepts

Hannover Medical School2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2026年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
5
试验地点
2
主要终点
Pitch perception performance of ANI

研究概览

简要总结

The objective of this scientific study is to evaluate the feasibility of direct auditory nerve stimulation to elicit key percepts, specifically loudness and frequency/pitch percepts in three deaf patients participants with the new auditory nerve implant (ANI). During the year with temporary stimulation of the auditory nerve, patients participants are expected to participate for 14 months, consisting of: two months for surgery for the nerve implant and healing phase, one month initial follow-up, ten months of follow-up care and study testing, and one month for explanation and post-operative observation.

详细描述

The auditory nerve implant (ANI) targets the auditory nerve directly between the cochlea and the brainstem, whereas current implants like the cochlear and brainstem implants stimulate the cochlea or brainstem, respectively. By providing direct stimulation within the auditory nerve, a nerve implant offers a better electrode-nerve interface and may achieve improved hearing compared to a cochlear or brainstem implant. Preliminary results in animals, computer simulations, and acute clinical studies showed significantly better performance compared to other hearing aidsoptions. This study aims to investigate the extent to which these benefits are perceptible in the human auditory nerve.

The primary goal of this study is to gain scientific insight into the hearing experience with the direct auditory nerve stimulation. However, the results could contribute to the development of new hearing implants that directly stimulate the auditory nerve.

研究设计

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

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥18 and ≤85 years
  • Written informed consent
  • Bilateral deafness with cochlea that does not allow the implantation of a cochlear implant (CI). This can include ossification, malformation of cochlea; poor CI performers (lowest quartile of CI performance); and patientparticipants with facial nerve stimulation using a CI which is not manageable without reduction of performance
  • Eligible for routine auditory brainstem implant (ABI) where patientparticipants would undergo more invasive brainstem surgery than the ANI surgery
  • Functional auditory nerve and central auditory pathway
  • Post-linguistic onset of ipsilateral severe-to-profound hearing loss
  • The contralateral ear has sufficient vestibular function
  • Women not able to become pregnant*
  • Women not able to become pregnant defined as follows:
  • at least 6 weeks after surgical sterilization by bilateral tubal ligation or bilateral oophorectomy or
  • hysterectomy or uterine agenesis or
  • ≥ 50 years and in postmenopausal state > 1 year or
  • < 50 years and in postmenopausal state > 1 year with serum FSH > 40 IU/l and serum estrogen < 30 ng/l or a negative estrogen test, both at screening

排除标准

  • Medical, neurological, or psychological conditions that would contraindicate undergoing surgery, e.g. depression, acute cardiac infarction, history of stroke, dementia, epilepsy
  • Additional handicaps that would prevent participation in evaluations
  • Women able to become pregnant
  • Pregnant women
  • Persons who are deprived of their liberty on the basis of an official order or a court order or authorization
  • Known allergies to one of the components of the implant (medical grade silicone, Parylene-C, Iridium oxide, Platinum-Iridium alloy (PtIr 10) and (PtIr 20) )
  • Other active devices with potential interference with the auditory nerve implant
  • Presence of anatomic abnormalities that would prevent appropriate placement of the stimulator housing in the bone of the skull
  • Additionally, in the event of other health issues, the investigators will decide on a case-by-case basis whether to enroll the patientparticipant in the study

结局指标

主要结局

Pitch perception performance of ANI

时间窗: 12 months

Systematic place pitch ordering maintained on month 12

次要结局

  • Loudness perception performance of ANI(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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