Restore Claims Characterization Study

Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome Clinical Trial

Official title: Restore Claims Characterization Study

Status Completed

Clinical Trial Summary

The purpose of this study is to characterize the pain coverage capability of the RESTORE spinal cord stimulation (SCS) and assess health outcomes.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome
• Complex Regional Pain Syndromes
• Failed Back Surgery Syndrome
• Pain, Intractable
• Reflex Sympathetic Dystrophy

• NCT number: NCT00200122
• Study type: Interventional
• Source: MedtronicNeuro
• Status: Completed
• Phase: Phase 4
• Start date: January 2005
• Completion date: August 2007