Comparison of three paradigms for deep brain stimulation programming in the nucleus subthalamicus in Parkinson's disease patients
Not Applicable
Recruiting
- Conditions
- G20.1
- Registration Number
- DRKS00030350
- Lead Sponsor
- niversitaetsklinikum Wuerzburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Diagnosis of idiopathic Parkinson's disease, Implantation of deep brain stimulation with directional sensing electrodes in the subthalamic nucleus at least three months prior, Written informed consent for study participation, Complete preoperative imaging.
Exclusion Criteria
Concomitant diseases that may interfere with the focus of the study (especially severe underlying diseases, severe neurological or psychiatric concomitant diseases), lack of written consent to participate in the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Differences in symptom control and time for programming (TFP) between different programming paradigms
- Secondary Outcome Measures
Name Time Method Prespecified secondary endpoints were differences in total electrical energy delivered (TEED), rate of side effects, and stimulation parameters (i.e., amplitude, frequency, pulse width).