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Longitudinal Outcomes in MED-EL Cochlear Implant Recipients Using a FLEX Electrode

Active, not recruiting
Conditions
Cochlear Implants
Registration Number
NCT06343571
Lead Sponsor
MED-EL Elektromedizinische Geräte GesmbH
Brief Summary

This retrospective study aims at analysing data from clinical routine as anonymized data sets. The study aims at analysing clinical data from MED-EL Cochlear Implant (CI) recipients using a FLEX electrode array.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
2000
Inclusion Criteria
  • MED-EL CI recipients
  • FLEX electrode array
Exclusion Criteria
  • Lack of compliance with any inclusion criterion

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluate short and long term longitudinal clinical performance data from MED-EL CIs to assess their clinical effectiveness and safety.Through study completion: single data extraction (3 month to completion)

Longitudinal data from clinical routine

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hannover Medical School

🇩🇪

Hanover, Germany

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