Study Title
PRECISION RETROSPECTIVE OUTCOMES (PRO)
Purpose
Observational
This is an observational study which will evaluate de-identified (anonymous) data in subject medical charts to review the clinical outcomes of spinal cord stimulation.
Eligibility
Patients that underwent spinal cord stimulator trial and/or permanent implant of a Boston Scientific device.
Study Process
This study will evaluate de-identified (anonymous) data in subject medical charts to review the clinical outcomes of spinal cord stimulation. Data will be collected from medical chart review of subjects that have been implanted with a Boston Scientific spinal cord stimulator. All personal identifiers will be removed.
Trial Details
Investigator:
Randall Brewer, MD, CPI
IRB:
Western
IRB Number:
Trial Type:
Drug
Sponsor:
Boston Scientific
Contact Information:
River Cities Clinical Research Center
(318) 212-3796
http://www.rcips.com