Udall Project 1 Aim 4

Status Recruiting

Clinical Trial Summary

Non-randomized data collection, excepting participants completing the "Implanted DBS Structured Data Collection", who will be randomized to one of two conditions.

Clinical Trial Description

Patients with movement disorders, for example Parkinson's disease (PD), essential tremor (ET) and dystonia, will be assessed using appropriate clinical and (sensor) quantified measures in order to obtain quantitative and qualitative data that is not consistently obtained in clinical exams. This data will aid in assessing trends and outcomes in motor and non-motor signs, side effects and symptoms that correlate with deep brain stimulation (DBS) lead location, stimulation parameters, and other variables, for those that have received this treatment, in order to inform neurosurgical and neurological practices aimed at optimizing treatment and therapy for movement disorders. For those patients that have received DBS lead implant(s), this study will include the analysis of patient's clinical and/or research-related intraoperative neurophysiological recordings collected during the microelectrode recording portion of the DBS lead implant surgery. Additionally, researchers may analyze trends and outcomes by gathering data from retrospective and prospective chart review ;

Study Design

Related Conditions & MeSH terms

Movement Disorders

Clinical Trial Details

NCT number	NCT05568199
Study type	Observational
Source	University of Minnesota
Contact	Niecy Beltz
Phone	612-626-5711
Email	beltz070@umn.edu
Status	Recruiting
Phase
Start date	March 5, 2024
Completion date	January 1, 2035

View Details

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