Z96.2
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Cochlear implantation performed within the defined study period (2013–2025) at the Department of Otorhinolaryngology–Head and Neck Surgery, Medical Center–University of Freiburg. Use of a multichannel cochlear implant electrode array from one of the following manufacturers: Cochlear™, MED-EL, or Advanced Bionics. Availability of complete clinical documentation, including surgical reports, intraoperative measurements, and follow-up records. Presence of intraoperative and/or postoperative assessment of electrode position, based on imaging modalities (DynaCT or digital volume tomography [DVT]) and/or intraoperative electrophysiological measurements (e.g., transimpedance matrix [TIM]).
Exclusion criteria
Exclusion criteria: Incomplete or missing clinical documentation, particularly absent surgical reports, intraoperative measurement data, or follow-up records. Missing or non-evaluable intraoperative and/or postoperative imaging, or imaging that did not allow reliable assessment of electrode position.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of this study is to investigate how cochlear morphology, insertion angle and depth, scalar position, and the location of the first electrode artifact—considering different electrode array designs—affect speech perception and hearing outcomes following cochlear implantation. In addition, differences between primary implantations and reimplantations, patients with residual hearing, and age-related effects in patients younger and older than 70 years will be analyzed. | — |
Countries
Germany