Intraoperative Microelectrode Recordings Using MAVEN Compared to Standard Recording Apparatuses

StatusRecruiting
PhaseNot specified
Started

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Record History

  1. Study First Submitted
Mayo Clinic
1,024 trials monitored
See 128 trials at risk
Parkinson's Disease
1,462 trials monitored
See 71 trials at risk
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.
Trial Details
NCT Number NCT07868614
Lead Sponsor Mayo Clinic
Conditions
(from sponsor)		 Essential Tremor, Parkinson's Disease, Dystonia
Related terms Dystonia, Essential Tremor, Parkinson Disease
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov