To evaluate DBS device settings and match with the features of the DBS care management software.
This is a study done on Parkinson disease subjects who have received the DBS system implanted in their subthalamic nucleus.
Study Type
OBSERVATIONAL
Enrollment
20
Advanced Parkinson's disease patients implanted with the Medtronic Deep Brain Stimulation (DBS) system.
Scripps Clinic, Division of Neurology
La Jolla, California, United States
Parkinson's Disease and Movement Disorder Center, University of Kansas Medical Center
Kansas City, Kansas, United States
To Characterize the Percentage of Leads in Which the Target Map and the Clinically-derived Activation Map Overlap
The one-sided 95% exact binomial lower confidence bound of the proportion was calculated from subjects with readable images enrolled in the study.
Time frame: 18 months
Additional Study Measure on Unified Parkinson's Disease Rating Scale (UPDRS) III Scores
The summary of UPDRS III medication off score at baseline and the UPDRS III stimulation on/medication off score at follow-up and the change from baseline to 18 months. The UPRS III has a range of 0 - 108.
Time frame: Change from baseline to 18 months
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