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Optimized Programming in Spinal Cord Stimulation (SCS) System

NCT00871819 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2013-11-27

Study results available
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Summary

The objective of this study is to evaluate extent, location, and perception of paresthesia as a function of anode/cathode configuration.

Conditions

  • Neuropathic Pain
  • Pain

Interventions

DEVICE

Precision Spinal Cord Stimulation (SCS)

Various SCS device programming parameters

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Nicholas Kormylo, MD · University of California, San Diego

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-03-31
Primary Completion
2009-08-31
Completion
2009-09-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT00871819 on ClinicalTrials.gov