Optimal Stimulation Programming for Spinal Peripheral Neuromodulation

Status Completed

Clinical Trial Summary

To determine the best parameters with various leads to cover back and leg pain and provide best pain relief

Clinical Trial Description

Prospective double-blinded trial of patients already implanted with SCS to determine which programming model best controls their back and or leg pain. Baseline visit is 2 weeks after implant. Baseline study data is collected, program #1 is started. The visit @ week 4 collects NRS, changes to program #2. The visit @ week 6 collect NRS, and starts program #3. The visit @ week 8 collects NRS. Subject chooses their preferred program from the previous 3 and uses that for the next 12 weeks. The visit @ week 20 collects NRS. ;

Study Design

Related Conditions & MeSH terms

Chronic Pain

Clinical Trial Details

NCT number	NCT02346383
Study type	Interventional
Source	Carolinas Center for Advanced Management of Pain
Contact
Status	Completed
Phase	N/A
Start date	September 2013
Completion date	June 2016

View Details

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