Study Title
ENVISION: RELIEF Study Cohort
Purpose
Collect long term follow up data from patients with a Boston Scientific spinal cord stimulator and to observe connection between certain objective measurements (heart rate, sleep data) and patient outcomes.
Eligibility
Existing patient of the practice currently implanted with a spinal cord stimulator to treat chronic low back pain and/or chronic leg pain OR with a treatment plan for implant.
Cannot: Be under age 18
Study Process
Study duration is one year
Trial Details
Investigator:
IRB:
Western
IRB Number:
Trial Type:
NA
Sponsor:
Boston Scientific
Contact Information:
WK River Cities Clinical Research Center