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Auditory Nerve Test System During Vestibular Schwannoma Resection (ANTS)

Primary Purpose

Vestibular Schwannoma, Acoustic Neuroma, Sensorineural Hearing Loss

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Auditory Nerve Test System
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Vestibular Schwannoma focused on measuring Cochlear implant, Vestibular schwannoma, Acoustic Neuroma, Sensorineural hearing loss, Asymmetric sensorineural hearing loss, Single-sided deafness, Auditory nerve

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Vestibular schwannoma (sporadic or Neurofibromastosis Type-2)
  • 12 years of age or older
  • Tumor size < 2.5 cm
  • Non-serviceable ipsilateral hearing
  • No prior cochlear implant or auditory brainstem implant use
  • No prior microsurgery or stereotactic radiation for this tumor
  • Patient decision and medical clearance for a translabyrinthine approach for tumor resection
  • Willingness to comply with research protocol
  • Reasonable expectations of cochlear implant performance
  • Auditory nerve integrity visually confirmed following tumor resection

Exclusion Criteria:

  • Pathology/tumors other than a vestibular schwannoma
  • Younger than 12 years of age
  • Tumor size > 2.5 cm
  • Serviceable hearing in the tumor ear
  • Prior cochlear implant use in either the contralateral or ipsilateral ear
  • Prior microsurgery or stereotactic radiation for this tumor
  • Unwilling to comply with research protocol
  • Auditory nerve integrity cannot be visually confirmed after tumor resection

Sites / Locations

  • Washington University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention Group

Arm Description

Patients undergoing a translabyrinthine approach for vestibular schwannoma resection will have the health of their auditory nerve monitored during tumor dissection. If the auditory nerve is visually confirmed to be intact, then concurrent cochlear implantation will be performed.

Outcomes

Primary Outcome Measures

Auditory Nerve Electrophysiology
Reliability of electrically-evoked direct auditory nerve monitoring at the brainstem (eCNAP) and far-field auditory brainstem response (eABR). The auditory nerve signal will be monitored before, during, and after vestibular schwannoma resection. Elements like signal amplitude, latency, and preservation of eABR waveforms III and V will be measured.

Secondary Outcome Measures

Cochlear Implant Speech Performance
Speech performance measured in the CI-only condition using CNC Words, AzBio Sentences in Quiet, and AzBio Sentences in +10 dB SNR.
Sound Localization
Using an audio booth that contains a sound arc, patients will be asked to identify where a sound is coming from in the implant-on and implant-off conditions. This ability to localize is measured with a root-mean-square (RMS) error rate.
Quality of Life Following Vestibular Schwannoma Resection
Diagnosis and treatment of vestibular schwannomas can impact multiple aspects of a patient's quality of life. Using patient-reported outcome measures these aspects will be measured throughout their treatment course. The specific questionnaires will be: Speech, Spatial and Qualities of Hearing (SSQ), Hearing Handicap Inventory for Adults (HHIA), Tinnitus Handicap Inventory (THI), Dizziness Handicap Inventory (DHI), Penn Acoustic Neuroma Quality of Life (PANQOL), Cochlear Implant Quality of Life (CIQOL).

Full Information

First Posted
November 5, 2019
Last Updated
December 8, 2022
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04241679
Brief Title
Auditory Nerve Test System During Vestibular Schwannoma Resection
Acronym
ANTS
Official Title
Feasibility of Auditory Nerve Test System for Optimization of Simultaneous Translabyrinthine Vestibular Schwannoma Resection With Cochlear Implantation
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 20, 2020 (Actual)
Primary Completion Date
November 30, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The Auditory Nerve Test System (ANTS) is a novel device that stimulates the auditory nerve much like a cochlear implant. The purpose of this study is to demonstrate feasibility of the ANTS during translabyrinthine surgery for vestibular schwannoma resection. If the auditory nerve is kept intact, then the patients will also receive a cochlear implant at the same time potentially alleviating the morbidities caused by a vestibular schwannoma and asymmetric sensorineural hearing loss.
Detailed Description
Many patients diagnosed with a vestibular schwannoma (also called acoustic neuroma) eventually lose hearing in the afflicted ear. Improvements in magnetic resonance imaging (MRI) have led to tumors being diagnosed at smaller sizes, however, this has not changed the eventual demise in hearing for most patients. Hearing loss leads to tinnitus, poor sound localization, difficulty hearing in background noise, and imbalance all of which contribute to the decreased quality of life associated with a vestibular schwannoma diagnosis. Some tumors may be resected while maintaining the integrity of the auditory nerve. When a patient has hearing, the health of the auditory nerve can be monitored during the surgery through auditory-evoked (sound) measurements. When a patient has already lost their hearing or the surgical approach sacrifices all residual hearing, then auditory-evoked measurements can no longer be used and there is no way to monitor the auditory nerve aside from visual inspection. The Auditory Nerve Test System (ANTS) is a novel device designed to facilitate electrically-evoked auditory nerve monitoring. The ANTS is comprised of three parts: a test electrode, connector cable, and stimulator box. The test electrode functions like a mini-cochlear implant placed within the cochlea during a translabyrinthine surgery. During tumor resection the test electrode electrically stimulates the auditory nerve allowing surgeons to monitor electrophysiologic data on the health of the auditory nerve. The primary goal of this study is to assess the ANTS during translabyrinthine vestibular schwannoma resections. If patient are able to maintain an intact auditory nerve following vestibular schwannoma resection then a cochlear implant will be placed during the same surgery. Secondary outcomes measures will investigate cochlear implant outcomes and patient quality of life following this procedure and over the first year of using their cochlear implant. These secondary outcomes will be measured at 3-months, 6-months, and 12-months following cochlear implant activation. The test will assess how well the cochlear implant is working, the cochlear implant's impact on sound localization and hearing in background noise, and finally various aspects relevant to the patient's quality of life (tinnitus, balance, hearing, and overall quality of life).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Schwannoma, Acoustic Neuroma, Sensorineural Hearing Loss, Asymmetric Sensorineural Hearing Loss, Cochlear Nerve Damage, Cochlear Nerve Deafness, Skull Base Neoplasms, Auditory; Nerve
Keywords
Cochlear implant, Vestibular schwannoma, Acoustic Neuroma, Sensorineural hearing loss, Asymmetric sensorineural hearing loss, Single-sided deafness, Auditory nerve

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single arm study of 10 patients with no serviceable hearing due to small or medium sized vestibular schwannomas undergoing translabyrinthine resection.
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Patients undergoing a translabyrinthine approach for vestibular schwannoma resection will have the health of their auditory nerve monitored during tumor dissection. If the auditory nerve is visually confirmed to be intact, then concurrent cochlear implantation will be performed.
Intervention Type
Device
Intervention Name(s)
Auditory Nerve Test System
Intervention Description
The Auditory Nerve Test System provides an electrically-evoked signal from within the cochlea to facilitate intraoperative auditory nerve monitoring. The auditory nerve can be measured both at the root entry zone of the brainstem (eCNAP) and with scalp electrodes (eABR). Data on the health of the auditory nerve will be collected immediately prior to tumor dissection, during tumor dissection, and immediately after tumor dissection. The main purpose of this study is to determine feasibility of this novel intraoperative monitoring protocol. Secondarily, if the auditory nerve is visually confirmed to be intact following tumor resection then the patients will receive a cochlear implant during the same surgery.
Primary Outcome Measure Information:
Title
Auditory Nerve Electrophysiology
Description
Reliability of electrically-evoked direct auditory nerve monitoring at the brainstem (eCNAP) and far-field auditory brainstem response (eABR). The auditory nerve signal will be monitored before, during, and after vestibular schwannoma resection. Elements like signal amplitude, latency, and preservation of eABR waveforms III and V will be measured.
Time Frame
Intraoperative testing
Secondary Outcome Measure Information:
Title
Cochlear Implant Speech Performance
Description
Speech performance measured in the CI-only condition using CNC Words, AzBio Sentences in Quiet, and AzBio Sentences in +10 dB SNR.
Time Frame
3-months and 12-months after cochlear implant activation
Title
Sound Localization
Description
Using an audio booth that contains a sound arc, patients will be asked to identify where a sound is coming from in the implant-on and implant-off conditions. This ability to localize is measured with a root-mean-square (RMS) error rate.
Time Frame
Initial cochlear implant activation, then repeated at 6-months and 12-months after activation.
Title
Quality of Life Following Vestibular Schwannoma Resection
Description
Diagnosis and treatment of vestibular schwannomas can impact multiple aspects of a patient's quality of life. Using patient-reported outcome measures these aspects will be measured throughout their treatment course. The specific questionnaires will be: Speech, Spatial and Qualities of Hearing (SSQ), Hearing Handicap Inventory for Adults (HHIA), Tinnitus Handicap Inventory (THI), Dizziness Handicap Inventory (DHI), Penn Acoustic Neuroma Quality of Life (PANQOL), Cochlear Implant Quality of Life (CIQOL).
Time Frame
Pre-operative baseline, then 3-months and 12-months post-operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Vestibular schwannoma (sporadic or Neurofibromastosis Type-2) 12 years of age or older Tumor size < 2.5 cm Non-serviceable ipsilateral hearing No prior cochlear implant or auditory brainstem implant use No prior microsurgery or stereotactic radiation for this tumor Patient decision and medical clearance for a translabyrinthine approach for tumor resection Willingness to comply with research protocol Reasonable expectations of cochlear implant performance Auditory nerve integrity visually confirmed following tumor resection Exclusion Criteria: Pathology/tumors other than a vestibular schwannoma Younger than 12 years of age Tumor size > 2.5 cm Serviceable hearing in the tumor ear Prior cochlear implant use in either the contralateral or ipsilateral ear Prior microsurgery or stereotactic radiation for this tumor Unwilling to comply with research protocol Auditory nerve integrity cannot be visually confirmed after tumor resection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cameron C Wick, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Auditory Nerve Test System During Vestibular Schwannoma Resection

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