Comparative study of experimentally observed effects of DBS in STN or GPi in Parkinon*s patients for different stimulation amplitude-frequency combinations.
Completed
- Conditions
- Parkinson's disease10028037
- Registration Number
- NL-OMON31600
- Lead Sponsor
- Medisch Spectrum Twente
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 128
Inclusion Criteria
- Parkinson patients receiving DBS in the STN or GPi
- Patients underwent surgery at least three month ago
- Patients experiencing good clinical results from DBS
- Patients do not experience major fluctuations in symptoms due to medication
- Patients are in good physical condition
- Patients responding within 5 minutes to changes in the stimulator settings
Exclusion Criteria
- Patients who cannot fully cooperate during the experiments
- Patients suffering from dementia
- Patients suffering from severe dyskinesia
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method