Single-sided Deafness
Conditions
Keywords
deaf adult, single-sided, cochlear implant
Brief summary
The purpose of this investigation is to determine the safety and preliminary efficacy of implanting a cochlear implant (CI) in the profoundly deaf ear of an adult with one normal hearing (NH) ear (termed single-sided deaf person, or SSD). The potential subjects will have been deafened post-lingually, thus, at one point the now deafened ear did conduct sound from the periphery. The MED-EL CI system will be implanted in ten (10) SSD patients.The long-term goal of this research program is to determine whether the CI, in combination with the NH ear, may provide improved localization ability and better speech understanding in noise, relative to performance before cochlear implantation (i.e., with the NH ear alone). A secondary long-term goal is to determine whether CI stimulation may reduce tinnitus severity, compared to tinnitus experienced prior to cochlear implantation or when the CI is turned off, after implantation.
Interventions
DEVICEMED-EL Maestro Cochlear Implant
cochlear implant
Sponsors
Med-El Corporation
House Clinic, Inc.
University of California, Los Angeles
Robert Shannon
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Is an adult (18 years of age or older) * English as the primary language * Able to undergo general anesthesia, as determined by physical examination and written report from the physician * Receives pneumovax vaccine within 2 weeks of surgery and provides documentation to the principal investigator * Profoundly/severely deaf in one ear (implant ear), as defined by: * 3-frequency pure-tone average≥70 dB Hearing Loss * Bone conduction thresholds consistent with air conduction thresholds (i.e., no conductive component to the hearing loss) * HINT sentence recognition score ≤40% correct, 60 dBA presentation level * Post-lingual onset of hearing loss, i.e., after age 6 years of age * Hearing loss occurred \<10 years prior, as obtained by history * Normal hearing in one ear (non-implant ear), as defined by: * 3-frequency PTA ≤25 dB HL * No tested frequency air conduction threshold \>35 dB HL * Bone conduction thresholds consistent with air conduction thresholds * Word recognition score ≥80% correct, 60 dBA presentation level * HINT sentence recognition score ≥ 80%, 60 dBA presentation level * Provides informed consent * Willing and able to follow the study protocol
Exclusion criteria
* Retrocochlear pathology resulting from Neurofibromatosis 2, or other types of cranial nerve/brainstem tumors * Co-existing medical conditions that require radiotherapy of the brainstem and/or auditory cortex * Any medical contraindication precluding safe administration of general anesthesia, e.g., * Cardiopulmonary disease * Renal disease * Otologic conditions which contraindicate surgery * Active middle ear infection * Tympanic membrane perforation * Anatomic abnormalities detected on CT preventing appropriate placement of the stimulator housing in the bone of the skull or placement of the electrode array in the cochlea (e.g., ossification) * Psychological conditions contraindicating surgery * Skin or scalp conditions that may preclude attachment of the coil or that may interfere with the use of the coil * Chronic pain in or around the head * Current or previous use of an active hearing implant (e.g., bone-anchored hearing aids, cochlear implant, etc.) * Developmental delays or organic brain dysfunction
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pure-tone threshold average (dB) | 6 months post-activation | Change in 3-frequency pure-tone threshold average (dB) in the normal hearing ear. |
| Hearing in Noise Test (signal-to-noise ratio) | 6 months post-activation | Change in Hearing in Noise Test signal-to-noise ratio in the normal hearing ear. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Adverse Events | 1-month post-implantation | Number of unexpected serious adverse events across all 10 subjects. |
Countries
United States
Outcome results
None listed