Clinical Research Directory

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