Personalized cochlear implant supply and anatomy-based adaptation of the cochlear implant with Otopla
Recruiting
- Conditions
- H90.3H93.1Sensorineural hearing loss, bilateralTinnitus
- Registration Number
- DRKS00026072
- Lead Sponsor
- Charité Campus Virchow-Klinikum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
• Patients who, according to the guidelines for cochlear implants of the German Society for Ear, Nose and Throat Medicine, Head and Neck Surgery e. V. have an indication for CI fitting from October 2020
• Residual hearing with a hearing threshold in tone threshold audiometry of <80 dB low tone (500 Hz).
Exclusion Criteria
none
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome - the health-related quality of life (NCIQ) - will be measured one week before the implantation, six and twelve months after the cochlear implantation.
- Secondary Outcome Measures
Name Time Method