Patient Retrospective Outcomes (PRO)

  • End date
    Dec 15, 2027
  • participants needed
  • sponsor
    Boston Scientific Corporation
Updated on 15 October 2021
chronic pain
spinal cord


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.


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.

Condition Pain, Chronic Pain, Post-Surgical Pain, Pain (Pediatric), chronic pains
Treatment Non Boston Scientific spinal cord stimulation system, Boston Scientific Precision Plus spinal cord stimulation system, Non-spinal cord stimulation conventional medical management for chronic pain, Boston Scientific Spinal Cord Stimulation Systems, Non Boston Scientific Systems, Boston Scientific Systems
Clinical Study IdentifierNCT01550575
SponsorBoston Scientific Corporation
Last Modified on15 October 2021


Yes No Not Sure

Inclusion Criteria

Previously treated with or eligible for use with Boston Scientific Systems
years of age or older at the start of Baseline
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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