High-density in Spinal Cord Stimulation: Virtual Expert Registry

NCT02787265 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 272

Last updated 2021-02-01

No results posted yet for this study

Summary

This is a prospective, multi-center, observational follow-up study observing the effectiveness of high density spinal cord stimulation in patients with failed back surgery syndrome patients with back and leg pain.

Conditions

  • Failed Back Surgery Syndrome

Interventions

DEVICE

spinal cord stimulation

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY
  • Universitair Ziekenhuis Brussel

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2020-12-08
Completion
2020-12-08

Countries

  • Belgium

Study Locations

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Entities

Companies

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 NCT02787265 on ClinicalTrials.gov