H91.9
Conditions
Interventions
Group 1: The primary purpose of the study is exploration and feasibility testing. A drill path is calculated using pre-operative data, which is checked for accuracy during conventional CI implantation
Sponsors
Universitätsklinik für Hals-Nasen-Ohrenheilkunde
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who have decided to undergo CI implantation following the preliminary CI examination at the University ENT Clinic Oldenburg.
Exclusion criteria
Exclusion criteria: Patients who are at increased risk for inner ear malformations.Patients who have an increased risk during anesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Verification of the accuracy of the drill path calculated by the planning software after conventional CI surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcomes | — |
Countries
Germany
Contacts
Public ContactAndreas Radeloff
Universitätsklinik für Hals-Nasen-Ohrenheilkunde
Outcome results
None listed