Hearing Loss, Cochlear, Hearing Loss, Sensorineural
Conditions
Keywords
hearing preservation, cochlear implant, intracochlear catheter, steroids, INCAT, sensorineural hearing loss
Brief summary
This is a feasibility study for a inner ear catheter which will be used to apply steroids to the inner ear. It will be used on nearly deaf patients during their surgery, when they receive an implant that will restore the hearing. Treatment with steroids will improve the maintenance of residual hearing, which will be tested during and after the surgery.
Detailed description
Study Device: The INCAT is an intracochlear catheter which is eligible in Canada for intracochlear drug delivery. Summary: 24 patients with moderate to profound hearing loss and indication for cochlear implantation will receive intracochlear treatment with steroids with an intracochlear catheter (INCAT) for hearing preservation prior to insertion of the cochlear implant array. Subjects will be considered for the study if they are 18 years of age or older and demonstrate a CNC word score in quiet of 60% or less in the ear to be implanted. Subjects will be followed for 6 months post-activation of the audio processor. Primary Objectives: Determination of feasibility of the intracochlear catheter INCAT and hearing preservation of residual hearing thresholds intra-, postoperatively, and long-term. Secondary Objectives: Assessment of quality of life, tinnitus and development of speech perception with the implant up to one year after implantation. Study Endpoint: Feasibility of using the INCAT and assessment of hearing preservation of residual hearing thresholds. Impedance field telemetry will help to assess hearing thresholds pre-, peri-, and postinsertion.
Interventions
DEVICEintracochlear catheter
intracochlear administration of steroids through the intracochlear catheter INCAT
Sponsors
Sunnybrook Health Sciences Centre
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
feasibility study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adults, 18 years of age or older at the time of implantation * Moderate to profound hearing loss in the low frequencies and severe to profound hearing * Loss in the high frequencies, bilaterally as defined by (see Figure 4A and B below for example audiogram information) * Low-frequency pure tone average (PTA - 250, 500, and 1000 Hz) greater than 40 dB * High-frequencies not better than 65 decibels (3000 Hz - 8000 Hz) * Sensorineural hearing loss, demonstrated by an air-bone gap of less than or equal to 10 dB * Limited benefit from appropriately fit hearing aids, defined by consonant-nucleus-consonant (CNC) word score in quiet of 60% or less in the ear to be implanted and 70% or less in the non-implanted ear * CNC word score in quiet of greater than or equal to 10% in the ear to be implanted * Fluent in English * No radiological contraindications * Ability to undergo general anesthesia * Appropriate motivation and expectation levels * Stated willingness to comply with all study procedures for the duration of the study * Able to perform subjective hearing tests * Able to fill out questionnaires
Exclusion criteria
* Age less than 18 years * Not willing to provide informed consent * Unable to perform subjective hearing tests * Unable to fill out questionnaires * Previous unsensitivity to the investigated drug * Unable to follow the protocol for any reasons * Evidence that hearing loss is retrocochlear in origin * Active middle ear infection * Skin or scalp condition precluding use of external audio processor * Suspected cognitive impairment or organic brain dysfunction * History of prior use of a hearing implant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pure tone average with air and bone conduction | 12 Months | air and bone conduction of the frequencies 0.25, 0.5, 1, 2, 4, 6, 8 kHz |
| speech audiometry | 12 months | CNC, AzBio, HINT |
| Impedance | 12 months | Impedance testing for all electrodes |
| ECAPs | 12 months | electrically evoked compound action potential testing for all electrodes |
| ECochG | 12 months | electrocochleargraphy |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Tinnitus | 12 Months | Assessment of tinnitus with Tinnitus Handicap Inventory, which is a 25-item self-report measure to determine perceived tinnitus handicap severity |
Countries
Canada
Contacts
Primary ContactTrung Le, MD, PhD
Outcome results
None listed