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NCT07868614
Intraoperative Microelectrode Recordings Using MAVEN Compared to Standard Recording Apparatuses
Conditions: Essential Tremor, Parkinson's Disease, Dystonia
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 30
Sponsor: Mayo Clinic
Location: Mayo Clinic Rochester Minnesota
Summary
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.
Eligibility Criteria
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.
Source: ClinicalTrials.gov (NCT07868614). StuddyBuddy aggregates publicly available trial information.