Optimal Electrode Configuration of the MedEl Flex 28

Overview

About this study

The purpose of this study is to determine if adults using the MedEL Flex 28 cochlear implant derive greater benefit from temporal cues when they are coded by fewer numbers of apical electrodes.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adults implanted with the MedEl Flex 28 or standard array with at least 10 active electrodes
  • Patients with more than 6-months of implant use
  • Postlingually deafened

Exclusion Criteria:

  • Patients with known cognitive deficits
  • Patients less than 18 years of age
  • Patients with prelingual deafness

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Douglas Sladen, Ph.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

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Phone: 800-664-4542 (toll-free)

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