A Study to Evaluate the Effect of Precision Spectra™ Programming Features and Lead Options on Patient Outcomes (COVERAGE)
Chronic Pain
About this trial
This is an interventional other trial for Chronic Pain focused on measuring stimulation, implantable, pulse generator, back pain, chronic pain, leg pain
Eligibility Criteria
Inclusion Criteria:
- Meets RELIEF Registry criteria for inclusion
- Primary complaint of persistent or recurrent low back pain, with or without leg pain
- Signed a valid, IRB/EC-approved informed consent form
Exclusion Criteria:
- Meets any RELIEF Registry criteria for exclusion
Sites / Locations
- Physicians Research Group, LLC
- Albany Medical Center
- PCPMG Clinical Research Unit, LLC
- Spine Team Texas
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Conventional Programming, then Advanced Programming
Advanced Programming, then Conventional Programming
Precision Spectra SCS System with CoverEdge Surgical Lead or more than 2 percutaneous leads. Subjects first received conventional single source programming followed by Precision Spectra SCS System advanced programming.
Precision Spectra SCS System with CoverEdge Surgical Lead or more than 2 percutaneous leads. Subjects first received Precision Spectra SCS System advanced programming followed by conventional single source programming.