H91.9
Conditions
Interventions
Group 1: Methods and timeline:
Study design and type:
monocentric, retrospective, non-randomized study with a prospective component.
Prospective part:
The NCIQ and Tinnitus Questionnaires where intr
Sponsors
Helios Center for Research and Innovationc/o Helios Klinik Cuxhaven
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - patients with a CI implantet at the medical center Helios München West - older than 18 years of age - willing and able to participate - good command of German for the understandig of questionnaires and speech test material
Exclusion criteria
Exclusion criteria: - younger than 18 years of age - lack of decision-making ability - no willingness to cooperate - revision surgery during the study participation - lack of sufficient command of German
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of subjective appraisal of cochlea implant provision using validated quality of life questionnaires with at least 60 CI recipients. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of predictive factors on the subjective success of the treatment (e.g. tinnitus suppression), rating of correlations between subjective success and audiometric test results. | — |
Countries
Germany
Contacts
Public ContactIoana Brill
Helios München West
Outcome results
None listed