Fundamental Asynchronous Stimulus Timing Sound Coding Study (FAST)
Sensorineural Hearing Loss
About this trial
This is an interventional treatment trial for Sensorineural Hearing Loss focused on measuring cochlear implant, sensorineural hearing loss
Eligibility Criteria
Inclusion Criteria
- Medical and audiological candidate for a unilateral CI24RE, CI512 or CI532 series implant
- Post-linguistically deafened
- Native speaker of American English
- Eighteen years of age or older
Exclusion Criteria
- Previous or existing cochlear-implant recipient
- Pre-linguistically deafened (onset of hearing loss at less than two years of age)
- Ossification or any other cochlear anomaly that might prevent complete insertion of the electrode array
- Diagnosis of retro-cochlear pathology
- Diagnosis of auditory neuropathy
- Unrealistic expectations on the part of the subject regarding the possible benefits, risks, and limitations that are inherent to the surgical procedure and use of the prosthetic device
- Unwillingness or inability to comply with all investigational requirements
- Additional cognitive handicaps that would delay rate of improvement with the cochlear implant
Sites / Locations
- University of Colorado Health
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Group 1
Group 2
All patients will be receiving commercially available Cochlear™ Nucleus® CI24RE with Contour Advance™ Electrode or Cochlear™ Nucleus® CI512 cochlear implant with Contour Advance™ Electrode for this study. Group 1 will be receiving the FAST (experimental) sound coding strategy at initial activation and use it for the first three months.At the three month interval subjects in Group 1 will be switched to the commercially available ACE (control) sound coding strategy.
All patients will be receiving commercially available Cochlear™ Nucleus® CI24RE with Contour Advance™ Electrode or Cochlear™ Nucleus® CI512 cochlear implant with Contour Advance™ Electrode for this study. Group 2 will be the commercially available ACE (control) sound coding strategy at initial activation and use it for the first three months.At the three month interval subjects in Group 2 will be switched to the receiving intervention of the FAST (experimental) sound coding strategy. The experimental sound coding strategy will be used from 3-6 months post activation.