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Comparison of Senza to Commercial Spinal Cord Stimulation for the Treatment of Chronic Pain

NCT01609972 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 356

Last updated 2015-07-02

No results posted yet for this study

Summary

The purpose of this investigational study is to establish the safety and effectiveness of electrical stimulation delivered to the spinal cord in subjects with chronic, intractable pain of the trunk and/or limbs and will be a comparison of the Senza System with commercially available SCS systems.

Conditions

  • Chronic Low Back Pain

Interventions

DEVICE

Spinal Cord Stimulator

Non-inferior comparison of implantable spinal cord stimulators

Sponsors & Collaborators

  • Nevro Corp

    lead INDUSTRY

Principal Investigators

  • Leonardo Kapural, MD · The Center for Clinical Research, Winston-Salem, NC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2015-05-31
Completion
2015-06-30

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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 NCT01609972 on ClinicalTrials.gov