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Spinal Cord Stimulation (SCS) Therapy Study

NCT02371122 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2015-07-10

No results posted yet for this study

Summary

The purpose of this study is to evaluate the effect of different spinal cord stimulation settings in the treatment of leg pain. Subjects will receive a randomized order of four different programmed stimulation settings for 3 weeks each followed by a fifth and final setting.

Conditions

  • Failed Back Surgery Syndrome
  • Degenerative Disk Disease
  • Epidural Fibrosis
  • Arachnoiditis
  • Radiculopathies

Interventions

DEVICE

Therapy Setting 1 (Medtronic)

RestoreSensor or RestoreUltra Setting 1

DEVICE

Therapy Setting 2 (Medtronic)

Medtronic RestoreSensor or RestoreUltra Setting 2

DEVICE

Therapy Setting 3 (Medtronic)

Medtronic RestoreSensor or RestoreUltra Setting 3

DEVICE

Therapy Setting 4 (Medtronic)

Medtronic RestoreSensor or RestoreUltra Setting 4

Sponsors & Collaborators

  • MedtronicNeuro

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2016-11-30
Completion
2017-01-31

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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 NCT02371122 on ClinicalTrials.gov