Overview
The purpose of the study is to investigate the effect of an anatomy-based frequency distribution in comparison to a default frequency distribution in bimodal CI patients, i.e. wearing a cochlear implant and a contralateral hearing aid. Speech perception in quiet, speech perception in noise, consonant/vowel discrimination and pitch/timbre perception will be assessed in an acute set-up with both the default fitting map and the anatomy-based fitting map.
Eligibility
Inclusion Criteria:
- Age ≥ 18 years
- Post-lingual onset of severe to profound sensory-neural hearing loss in the implanted ear(s)
- Post-operative Computed Tomography (CT) scan of the CI electrode available
- Subject implanted with MED-EL cochlear implant(s)
- Subject received a Flex28, FlexSoft or Standard electrode
- Subject uses a SONNET 2 or RONDO 3 audio processor
- Subject has experience of at least 6 months with cochlear implant
- The most apical active electrode contact has to be inserted at least 540°
- Minimum of 10 active channels are activated
- Subject wears an adequately fitted hearing aid on the contralateral side
- Fluent in the language of the test centre
- Signed and dated Informed Consent Form (ICF) before the start of any study-specific procedure
Exclusion Criteria:
- Lack of compliance with any inclusion criteria
- Implanted with C40+, C40X and C40C
- Implanted with an Auditory Brainstem Implant (ABI) or Split electrode array
- Anything that, in the opinion of the Investigator, would place the subject at increased risk or pre-clude the subject's full compliance with or completion of the study
