Prospective, non-randomized, open-label study to evaluate the safety and efficacy of the iotaSOFT Insertion System when used to assist electrode array insertion during cochlear implant surgery in a pediatric population.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
robotic assistive technology for cochlear implant electrode insertion
University of Iowa
Iowa City, Iowa, United States
Texas Childrens Hospital
Houston, Texas, United States
Safety related to adverse events
Evaluation of iotaSOFT related adverse events and serious adverse events through 30 days after surgery
Time frame: 30 days following surgery
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