Patient Retrospective Outcomes (PRO)
ConditionChronic Pain
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBoston Scientific Corporation
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Previously treated with or eligible for use with Boston Scientific Systems
18 years of age or older at the start of Baseline
Disqualifiers
None
Trial population
Subjects who have previously been implanted with, or who are candidates for implantation with a spinal cord stimulation system or other various treatment approaches, such as radio frequency ablation or indirect decompression system (IDS).
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Non Boston Scientific Systems
DeviceSpinal cord stimulation, RF, IDS etc.
Boston Scientific Systems
DeviceSpinal cord stimulation, RF, IDS etc
Treatment groups
15,000 Participants
are divided into 2 treatment groupsGroup A: Patients eligible for SCS, RF or other treatment approaches2 interventions
Group B: Patients Eligible for treatment options with prior treatment2 interventions
Trial outcomes
Primary outcomes
1
Responder rate
Responder rate for pain relief through study completion.
Time frame
Through study completion, approximately two yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov