Mayo Clinic
The purpose of this research is to determine if the electrophysiologic data collected from standard-of-care microelectrode recordings during human deep brain stimulation (DBS) surgery will be the same using the MAVEN device compared with the standard Alpha Omega device with either a tungsten standard-of-care microelectrode (for microelectrode recordings), or a carbon-fiber microelectrode (for neurotransmitter recordings). The number of microelectrodes used for both the tungsten and the carbon-fiber version will be the same as the standard-of-care.
Inclusion Criteria: * Mayo Clinic patients already scheduled to undergo DBS surgery with Dr. Kendall Lee fora movement disorder. Exclusion Criteria: * Patients not approved for DBS surgery by the multidisciplinary DBS committee.
During deep brain stimulation (DBS) surgery, the MAVEN device will be used in parallel with the currently used Alpha Omega Device to compare the quality of electrophysiologic readings.
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