About this trial
The goal of the study is to determine the benefit of using an ECochG-based corrective action guide during cochlear implant surgery compared to the traditional surgical approach without ECochG surveillance and guidance.
Eligibility criteria
Qualifiers
Aged 18 years of age or older
Within cochlear implant inclusion criteria by local regulations/guidelines at the time of implantation
Severe to profound hearing loss (average air conduction unaided hearing threshold of ≥ 70 dB HL for 500, 1000, 2000 and 4000 Hz) in the ear to be implanted
Air conduction unaided hearing threshold ≤ 70 dB HL at 500 Hz in the ear to be implanted
Disqualifiers
Abnormal cochlear anatomy (including ossification) as identified by pre-operative radiological evaluation in the ear to be implanted
Any pre-existing cochlear or middle ear pathology, such as otosclerosis, cholesteatoma, or previous middle ear surgery in the ear to be implanted
Any medical conditions that would increase the risk of local complications during cochlear implantation, such as autoimmune diseases or active local infections
Diagnosis of auditory spectrum neuropathy disorder
Trial design
Treatments tested in this trial
- ECochG monitored CI surgery incl. corrective action guide
- Routine CI surgery without ECochG monitoring