Trial record 1 of 1 for:    NCT01864291
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Auditory Brainstem Implant (ABI) in Pediatric Non-Neurofibromatosis Type 2 Subjects

This study is currently recruiting participants. (see Contacts and Locations)
Verified October 2014 by Massachusetts Eye and Ear Infirmary
Sponsor:
Information provided by (Responsible Party):
Massachusetts Eye and Ear Infirmary
ClinicalTrials.gov Identifier:
NCT01864291
First received: May 22, 2013
Last updated: October 9, 2014
Last verified: October 2014

May 22, 2013
October 9, 2014
May 2013
November 2022   (final data collection date for primary outcome measure)
ABI Complications [ Time Frame: 5 years from date of surgery ] [ Designated as safety issue: Yes ]
We will track any major and minor complications peri-operatively and post-operatively in all study participants. Major complications include mortality, cerebellar contusion, facial palsy, meningitis, lower cranial neuropathy, hydrocephalus, pseudomeningocele and CSF leak. Minor complications include transient hydrocephalus, wound seroma, minor infections, balance problems, transient nerve palsies, transient dysphonia or difficulty swallowing, headache, flap problems, and non-auditory side effects. These complications will be tracked through serial clinical exams as well as patient recorded questionnaires to determine the safety profile of ABI surgery.
Same as current
Complete list of historical versions of study NCT01864291 on ClinicalTrials.gov Archive Site
  • Audiologic Performance with ABI [ Time Frame: 5 years from date of surgery ] [ Designated as safety issue: No ]

    We will complete audiologic and speech based tests to determine performance before and after ABI surgery. In particular, pre- and post-operative behavioral audiometry and speech perception testing will be used.

    Audiometric testing will include:

    • Detection audiogram, aided and unaided individual ears
    • IT-MAIS or MAIS
    • LING 6 sound test (MLV)
    • ESP Low Verbal or Standard-Recorded if possible or MLV @ 60dB HL
    • PB-k words and phonemes- Recorded @ 60dB HL
    • CNC- 50 words @ 65dB SPL

    Speech and language assessment: MacArthur-Bates Communicative Development Inventories (CDIs) (56), Pre-School Language Scale, , Fourth Edition (PLS-5) Clinical Evaluation of Language Fundamentals Preschool, Second Edition (CELF-P2), Clinical Evaluation of Language Fundamentals, Fourth Edition (CELF-4), and the Goldman-Fristoe Test of Articulation.

  • ABI Electrophysiologic Measures [ Time Frame: 5 years from date of surgery ] [ Designated as safety issue: No ]
    We will measure and record the specific programmed parameters of the ABI device. Intraoperatively, evoked Auditory Brainstem Response (eABRs) will be recorded and saved. These tracings and data will be compared to the settings on activation to determine whether the same electrodes are appropriately positioned. In addition, we will record stimulation thresholds for each electrode and track those parameters over time. By following these measure, we will be able to capture how electrophysiologic parameters vary (if at all) over time.
Same as current
Not Provided
Not Provided
 
Auditory Brainstem Implant (ABI) in Pediatric Non-Neurofibromatosis Type 2 Subjects
Study of the Nucleus 24 Auditory Brainstem Implant in Pediatric Non-Neurofibromatosis Type 2

The purpose of this research study is to determine whether Auditory Brainstem Implant (ABI) can improve hearing in children who are deaf and cannot receive a cochlear implants.

The goal of this MEEI Auditory Brainstem Implant (ABI) research study is to find new ways to improve hearing in children who are deaf and cannot receive a cochlear implant. The ABI is a surgically placed bionic implant that converts sounds into electrical signals that are directly transmitted to the cochlear nucleus, the first auditory center of the brain. For many years, ABIs have improved the hearing of patients who are deaf due to brain tumors associated with a genetic syndrome called Neurofibromatosis Type 2 (NF2). However, a number of recent studies suggest that deaf patients who do not have NF2 and are not eligible for a cochlear implant may also benefit from placement of an ABI. These preliminary studies suggest that these non-NF2 or "nontumor" patients may actually have better outcomes after ABI surgery than patients suffering from NF2. Children appear to be particularly good candidates because of their developmental plasticity and in many studies, outcomes are more favorable in children that adults. Patients who do not have NF2 and are deaf due to abnormalities in their hearing nerves or inner ears from congenital malformations, infection, disease, or injury are not cochlear implant candidates and there are no other options to improve hearing in these cases except for the ABI. Thus, the purpose of our study is to carefully analyze whether ABI surgery improves the hearing and quality of life of non-NF2 children based on subjective and objective measures of their hearing before and after ABI surgery. In particular, we plan to study ABI outcomes in non-NF2 pediatric patients, characterize the parameters used on their devices, and determine the safety profile of ABIs in these patients.

Interventional
Not Provided
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Bilateral Hearing Loss for Causes Other Than Tumors
Device: Nucleus 24 Auditory Brainstem Implant (ABI)
Nucleus 24 Auditory Brainstem Implant (ABI) surgery followed by device activation, testing, and clinical assessment for five years following surgery.
Other Name: ABI, Nucleus 24, Cochlear Americas
Experimental: Non-NF2 ABI surgery
All subjects will be part of a single arm involving placement of the Nucleus 24 Auditory Brainstem Implant (ABI) device.
Intervention: Device: Nucleus 24 Auditory Brainstem Implant (ABI)

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
15
November 2022
November 2022   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Pre-linguistic hearing loss (birth-5 yrs.; age at ABI implantation 18 months-5yrs) with both:

    1. MRI +/- CT evidence of one of the following:

      • Cochlear nerve deficiency
      • Cochlear aplasia or severe hypoplasia
      • Severe inner ear malformation
      • Post-meningitis ossification
    2. When a cochlea is present or patent with a normally appearing cochlear nerve, lack of significant benefit from CI despite consistent use (>6 mo.)

      • No or limited speech perception ability (limited to pattern perception on closed set testing materials using the CI)
      • Lack of progress in auditory skills development
  2. Post-linguistic hearing loss (<18 yrs. of age) with both:

    1. Loss or lack of benefit from appropriate CI without the possibility for revision or contralateral implantation. Examples might include:

      • Post-meningitis ossification
      • Bilateral temporal bone fractures with cochlear nerve avulsion
      • Failed revision CI without benefit
    2. Previously developed open set speech perception and auditory-oral language skills
  3. No medical contraindications
  4. Willing to receive the appropriate meningitis vaccinations
  5. No or limited cognitive/developmental delays which would be expected to interfere with the child's ability to cooperate in testing and/or programming of the device, in developing speech and oral language, or which would make an implant and subsequent emphasis on aural/oral communication not in the child's best interest
  6. Strong family support including language proficiency of the parent(s) in the child's primary mode of communication as well as written and spoken English.
  7. Reasonable expectations from parents including a thorough understanding:

    • of potential benefits and limitations of ABI
    • of parental role in rehabilitation
    • that the child may not develop spoken language as a primary communication mode or even sufficient spoken language to make significant academic progress in an aural/oral environment
  8. Involvement in an educational program that emphasizes development of auditory skills with or without the use of supplementary visual communication.
  9. Able to comply with study requirements including travel to investigation sites and clinic visits.
  10. Informed consent for the procedure from the child's parents.

Exclusion Criteria:

  1. Pre- or post-linguistic child currently making significant progress with CI - This will be considered if a child is progressing along the expected speech reception hierarchy (SRI-Q) as detailed by Wang et al (50). Even for the very young children (18 months of age with 6 months of use), nearly all children with a good auditory signal from their CI will have reached ceiling effects on the IT-MAIS and have pattern perception beyond chance using the ESP (50). Moreover, there will evidence of improvement in these metrics over time.
  2. MRI evidence of one of the following:

    • normal cochlea and cochlear nerves or NF2
    • brainstem or cortical anomaly that makes implantation unfeasible
  3. Clear surgical reason for poor CI performance that can be remediated with revision CI or contralateral surgery rather than ABI.
  4. Intractable seizures or progressive, deteriorating neurological disorder
  5. Unable to participate in behavioral testing and mapping with their CI. If this appears to be an age effect, ABI will be delayed until we can be assured that the child will be able to participate, as reliable objective measures of mapping are currently not available for mapping these devices.
  6. Lack of potential for spoken language development. This will be considered the case when evidence of the following exist:

    • Severe psychomotor retardation, autism, cerebral palsy, or developmental delays beyond speech that would preclude usage of the device and oral educational development. Autism is a special case where there is the potential for delayed presentation. When early signs are considered present, we will request a comprehensive developmental assessment for further evaluation prior to considering routine evaluation.
  7. Unable to tolerate general anesthesia (cardiac, pulmonary, bleeding diathesis, etc.).
  8. Need for brainstem irradiation
  9. Unrealistic expectations on the part of the subject/family regarding the possible benefits, risks and limitations that are inherent to the procedure and prosthetic device.
  10. Unwilling to sign the informed consent.
  11. Unwilling to make necessary follow-up appointments.
Both
18 Months to 17 Years
No
Contact: Daniel J Lee, MD, FACS 617-573-3130 daniel_lee@meei.harvard.edu
Contact: Barbara S Herrmann, PhD, CCC-A 617-573-3266 barbara_herrmann@meei.harvard.edu
United States
 
NCT01864291
13-028H
Yes
Massachusetts Eye and Ear Infirmary
Massachusetts Eye and Ear Infirmary
Not Provided
Principal Investigator: Daniel J Lee, MD FACS MEEI/MGH
Massachusetts Eye and Ear Infirmary
October 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP