Quantifying various effects of closed-loop Spinal Cord Stimulation (SCS) on pathophysiological mechanisms in Complex Regional Pain Syndrome (CRPS); an explorative study
Recruiting
- Conditions
- complex regional pain syndrome10034606reflex sympathetic dystrophy
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
a subject must meet the standard Dutch Neuromodulation Society consensus
criteria for spinal cord stimulation and the following study criteria:,
- Over 18 year old
- Diagnosed with retractable unilateral, upper- or lower limp CRPS,
- Capable and willing to participate in the additional measurements.
Exclusion Criteria
- Pain of other aetiology in addition to CRPS,
- Previously failed neuromodulation treatment (SCS or DRG).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary study parameter is the change in pain intensity at the end of the<br /><br>study compared with baseline.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Changes between the end of the study and baseline on all other parameters will<br /><br>be assessed and reported as secondary endpoints for this study.</p><br>