Prospective comparison of clinical versus anatomically informed CONtact selECTion in subthalamic deep brain stimulation for Parkinson’s Disease
Not Applicable
- Conditions
- G20.1
- Registration Number
- DRKS00034229
- Lead Sponsor
- niversität zu Köln
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Bilateral implantation of directional electrodes for deep brain stimulation in the subthalamic nucleus on both sides at least ten weeks before the start of the study
- Unchanged Parkinson's specific medication for at least two weeks before
start of examination
Exclusion Criteria
- Insufficient image quality of perioperative clinical imaging (cMRI/cCT) for reconstruction of the individual electrode position
- Disabling postural instability
- Cognitive deficit relevant to everyday life
- Vestibular or orthopaedic comorbidity relevant to everyday life
- Levodopa dysregulation syndrome
- Inability or unwillingness of the patient to use the patient remote control to independently adjust the stimulation amplitude
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Subjective preference
- Secondary Outcome Measures
Name Time Method MDS-UPDRS III after 1 week of treatment (Movement Disorder Society - Unified Parkinson’s Disease Rating Scale Part 3)<br>Continuous Accelerometrics