Non Boston Scientific Systems
DeviceSpinal cord stimulation, RF, IDS etc.
NCT Number: NCT01550575
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Berwick Pain Management, Berwick, Australia
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Spinal cord stimulation, RF, IDS etc.
Spinal cord stimulation, RF, IDS etc
Time frame: Through study completion, approximately two years
Responder rate for pain relief through study completion.
Interested in participating?
Request InfoBoston Scientific Corporation
Industry
Acronym: PRO
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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