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Clinical Trials/NL-OMON47186
NL-OMON47186
Completed
Not Applicable

Technical innovations for fitting and rehabilitation of adult CI users - Technical innovations for CI users

VUmc0 sites82 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
hearing impairment
Sponsor
VUmc
Enrollment
82
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
VUmc

Eligibility Criteria

Inclusion Criteria

  • Patients aged 18 years or older (all study parts); Patients with at least 1 year of CI experience after activation (study parts I, II, III and IV with experienced CI users); Newly implanted CI patients who enrol in the clinic's standard rehabilitation program after cochlear implantation (study part IV with newly implanted CI patients); Patients with onset of severe hearing impairment after the age of 7 years (all study parts); Native Dutch speakers (study parts I, II and III); Fluent Dutch speakers (study part IV); Patients using a Nucleus 6 CP900 processor (study part IV); Patients using a Nucleus 6 CP900, Nucleus 7 CP1000 or Kanso CP950 processor (study part I); Patients using a nucleus 5 or 6 CP800 or CP900 processor and the Freedom implant, with full insertion and 22 active electrodes (study part II)

Exclusion Criteria

  • Disability which could interfere with the completion of the tests (i.e. psychiatric problems, dyslexia or severe health problems); Additional handicaps that may prevent participation in evaluations; Patients with deviating map parameters (i.e., number of maxima, or pulses per second (PPS) (additional criterion for study part II)

Outcomes

Primary Outcomes

Not specified

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