Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
completion around
Principal Investigator
by Charles J Limb, MD (ucsf)
Headshot of Charles J Limb
Charles J Limb

Description

Summary

The current standard of care for cochlear implants (CI) does not address the significant pitch-place mismatch that is inherent in cochlear implantation (see detailed description below). The present study uses postoperative Flat Panel (higher resolution than standard) CT imaging to measure where CI electrodes sit within an individual's cochlea; doing so allows for more accurate frequency mapping (and thus pitch perception). The hypothesis of this study is that long-term (1 year) use of CT image-based frequency maps, beginning on the first day of CI activation, will improve user performance in the areas of speech and music perception, as compared to the use of default programming settings.

Official Title

High Resolution CT Guided Cochlear Implant Programming

Details

Keywords

Cochlear Implants, Hearing Loss, Amusia, Music perception, Place-pitch mismatch, Place coding, Cochlear duct length, Flat panel computed tomography, Cochlear implant programming, Frequency allocation table, CT Guided Cochlear Implant Programming, CT-Based Program for First Year of CI Use

Eligibility

Location

  • University of California, San Francisco
    San Francisco California 94115 United States

Lead Scientist at University of California Health

  • Charles J Limb, MD (ucsf)
    Dr. Charles Limb is the Francis A. Sooy Professor of Otolaryngology – Head and Neck Surgery and the Chief of the Division of Otology, Neurotology and Skull Base Surgery at University of California, San Francisco. He is the Director of the Douglas Grant Cochlear Implant Center at UCSF and he is the Medical Director of Cochlear Implantation at UCSF Benioff Children's Hospital, Oakland.

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT04506424
Study Type
Interventional
Participants
About 19 people participating
Last Updated