- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07789665
Auditory Intranerve Stimulation Perceptual Study (ANI-NIH)
Scientific Assessment of Auditory Intranerve Stimulation Loudness and Pitch Percepts
연구 개요
상세 설명
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.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Hubert Lim, Prof.
- 전화번호: +16126264565
- 이메일: Hlim@umn.edu
연구 장소
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Hanover, 독일, 30625
- 모병
- Hannover Medical School
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연락하다:
- Karl-Heinz Dyballa
- 전화번호: +4917615328589
- 이메일: dybala.karl-heinz@mh-hannover.de
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부수사관:
- Rolf Salcher, Dr.
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부수사관:
- Max Timm, Dr
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부수사관:
- Waldo Nogueira, Prof.
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부수사관:
- Karl-Heinz Dyballa, Dr.
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수석 연구원:
- Thomas Lenarz, Prof.
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Hanover, 독일, 30625
- 모집하지 않고 적극적으로
- Service provider for the performance of surgical procedures: International Neuroscience Institute
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 장치 타당성
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Experimental: Direct Auditory Nerve Stimulation
Patients Participants will be implanted with an Auditory Nerve Implant (ANI) for one year to evaluate key perceptual measures of temporary direct auditory nerve stimulation.
Safety and efficacy will also be evaluated, as well as different speech perception capabilities.
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The investigational research device consists of a speech processor worn on the ear and an implant body with an electrode array.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Pitch perception performance of ANI
기간: 12 months
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Systematic place pitch ordering maintained on month 12
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12 months
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Loudness perception performance of ANI
기간: 12 months
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Collection of loudness growth functions (LGFs) across single electrodes that have a dynamic range greater than 6 dB and maintained on month 12
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12 months
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기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Frequency Resolution
기간: 12 months
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Minimum frequency specificity (i.e., current spread) of electrodes is narrower than 0.8 mm in bandwidth maintained on month 12
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12 months
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Position of ANI electrode array in auditory nerve
기간: 12 months
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Evaluation of the final position of the ANI electrode array.
The number of electrodes eliciting auditory activation will be measured.
The stability of the percepts elicited will also be measured.
Both of these measurements provide the stability of the electrode array implanted within the auditory nerve.
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12 months
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Collection of adverse events
기간: 12 months
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Collection of adverse events during the evaluation period
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12 months
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공동 작업자 및 조사자
수사관
- 수석 연구원: Thomas Lenarz, Prof., Hannover Medical School
- 수석 연구원: Amir Samii, Prof., International Neuroscience Institute Hannover
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 0000509678
- No.11979-BO-MPDG-M-2025 (기타 식별자: Ethics committee Hannover Medical School)
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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