Patient Retrospective Outcomes (PRO)
Overview
- Phase
- Not Applicable
- Intervention
- Non Boston Scientific Systems
- Conditions
- Chronic Pain
- Sponsor
- Boston Scientific Corporation
- Enrollment
- 15000
- Locations
- 227
- Primary Endpoint
- Responder rate
- Status
- Recruiting
- Last Updated
- 26 days ago
Overview
Brief Summary
This study will evaluate de-identified (anonymous) data in subject medical charts to review the clinical outcomes of various treatment approaches in the treatment of chronic pain.
Detailed Description
This study is a retrospective, multi-center, de-identified patient data review. The study will include multiple independent cohorts to evaluate clinical outcomes in different subgroups.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Previously treated with or eligible for use with Boston Scientific Systems
- •18 years of age or older at the start of Baseline
Exclusion Criteria
- Not provided
Arms & Interventions
Patients eligible for SCS, RF or other treatment approaches
Patients who have previously been implanted with, or are eligible for implantation with a spinal cord stimulation system or various other treatment approaches such as RF, IDS, etc.
Intervention: Non Boston Scientific Systems
Patients eligible for SCS, RF or other treatment approaches
Patients who have previously been implanted with, or are eligible for implantation with a spinal cord stimulation system or various other treatment approaches such as RF, IDS, etc.
Intervention: Boston Scientific Systems
Patients Eligible for treatment options with prior treatment
Patients who have previously been implanted with a spinal cord stimulation system or other various treatments, and have thereafter received a different form of chronic pain treatment such as a different SCS system, RF, IDS etc.
Intervention: Non Boston Scientific Systems
Patients Eligible for treatment options with prior treatment
Patients who have previously been implanted with a spinal cord stimulation system or other various treatments, and have thereafter received a different form of chronic pain treatment such as a different SCS system, RF, IDS etc.
Intervention: Boston Scientific Systems
Outcomes
Primary Outcomes
Responder rate
Time Frame: Through study completion, approximately two years
Responder rate for pain relief through study completion.