Opto-electrical Cochlear Implants (oCI)
Hearing Loss
About this trial
This is an interventional device feasibility trial for Hearing Loss focused on measuring deaf, neural stimulation with light, cochlear implant
Eligibility Criteria
Inclusion Criteria:
Criterion for inclusion of a patient is the requirement of the translabyrinthine approach for tumor removal. The surgical approach is determined by the tumor size, the tumor location and the remaining hearing of the patient. Criteria for a translabyrinthine approach are:
- the tumor grows in the pontine angle and the facial nerve is at risk for damage during the surgery because the tumor is already large and in close proximity of the facial nerve AND
- the tumor is larger than 2.5 cm AND
- Pure tone hearing thresholds are elevated by at least 50 dB AND
- Speech discrimination scores are 50% or less
Exclusion Criteria:
- adults unable to consent.
- individuals who are not yet adults (infants, children, teenagers).
- pregnant women.
- prisoners.
- vulnerable populations
Sites / Locations
- University of Miami
- Central DuPage Hospital Association
- University of Missouri
Arms of the Study
Arm 1
Experimental
electrical and optical hybrid stimulation stimulation
Patients with large tumors of the skull base, requiring a translabyrinthine craniotomy with sacrifice of their cochlea and vestibular system during the tumor resection may participate. A recording electrode will be placed on the round window, a cochleostomy will be created, and different Light delivery systems (LDSs) will be inserted into the cochlea. LDSs include angle polished optical fibers to determine the accuracy of the orientation of the radiation beam, and hybrid arrays of small optical sources and electrical contacts to evaluate electric-alone stimulation as a reference, and compare it to optic-alone and combined electrical and optical stimulation. Compound action potentials (CAPs) of the auditory nerve will be recorded.