iotaSOFT Insertion System
Devicerobotic assistive technology for cochlear implant electrode insertion
NCT Number: NCT06106373
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.
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Notify Me9 month–12 year
All sexes
Interventional
Not applicable
University of Iowa, Iowa City, Iowa, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
robotic assistive technology for cochlear implant electrode insertion
Time frame: 30 days following surgery
Evaluation of iotaSOFT related adverse events and serious adverse events through 30 days after surgery
iotaMotion, Inc.
Industry
iotaSOFT Insertion System for Use With Cochlear Implant Surgery in Pediatrics
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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