Assessing the accuracy and handling of a minimally invasive cochlear implantatio

Recruiting

• Conditions: H91.9; Hearing loss, unspecified

• Registration Number: DRKS00017816
• Lead Sponsor: niversitätsklinik für Hals-Nasen-Ohrenheilkunde

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-06-07
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Patients who have decided to undergo CI implantation following the preliminary CI examination at the University ENT Clinic Oldenburg.

Exclusion Criteria

Patients who are at increased risk for inner ear malformations.Patients who have an increased risk during anesthesia.

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Verification of the accuracy of the drill path calculated by the planning software after conventional CI surgery.

Secondary Outcome Measures

Name	Time	Method
There are no secondary outcomes