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Quality of Life Outcomes in Spinal Cord Stimulation

NCT03249922 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6

Last updated 2018-07-24

No results posted yet for this study

Summary

The investigators will be evaluating quality of life outcomes in patients who are undergoing routine spinal cord stimulator implant for uncontrolled pain. Patients will be evaluated pre and post-operatively for quality of life improvements, pain control, and functionality.

Conditions

  • Neuropathic Pain
  • Low Back Pain

Interventions

DEVICE

Spinal Cord Stimulation

Implantation of a spinal cord stimulator for the control of axial back or neuropathic pain.

Sponsors & Collaborators

  • Rutgers, The State University of New Jersey

    lead OTHER

Principal Investigators

Eligibility

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

Timeline & Regulatory

Start
2017-10-27
Primary Completion
2018-07-22
Completion
2018-07-22
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT03249922 on ClinicalTrials.gov