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A Study to Evaluate the Effect of Precision Spectra™ Programming Features and Lead Options on Patient Outcomes — COVERAGE  

Chronic Pain Clinical Trial

Official title:
COVERAGE - A Study to Evaluate the Effect of Precision Spectra™ SCS System's Programming Features and Lead Options on Patient Outcomes

Clinical Trial Summary

The study is a prospective, on-label, multi-center, blinded, randomized controlled trial with a cross-over design to evaluate the effect of Precision Spectra™ SCS System's programming features and lead options.

Clinical Trial Description

The study is a sub-study of RELIEF - A Global Registry to Evaluate Long-Term Effectiveness of Neurostimulation Therapy for Pain (NCT01719055). The treatment will consist of permanent implant of a Precision Spectra™ SCS IPG with either a 32 contact CoverEdge™ Surgical Lead or with more than 2 percutaneous leads after a successful trial. Programming features and lead options of the Precision Spectra™ SCS System will be evaluated up to 3 months post-IPG activation. Following completion of the 3 month visit, subjects will continue to be followed for up to 36 months per the study requirements of the RELIEF Registry. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02384096
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Terminated
Phase N/A
Start date February 2015
Completion date October 2016
View Details
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