Patient Retrospective Outcomes (PRO)

NCT01550575 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15000

Last updated 2026-05-06

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Non Boston Scientific Systems

Spinal cord stimulation, RF, IDS etc.

DEVICE

Boston Scientific Systems

Spinal cord stimulation, RF, IDS etc

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Natalie Bloom Lyons · Boston Scientific Neuromodulation Corporation

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-03
Primary Completion
2030-12-31
Completion
2030-12-31

Countries

  • United States
  • Australia
  • Belgium
  • France
  • Germany
  • Italy
  • Netherlands
  • Portugal
  • Puerto Rico
  • Spain
  • Sweden
  • Switzerland
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01550575 on ClinicalTrials.gov