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Clinical Trial Summary

The study will compare therapeutic efficacy of a novel spinal cord stimulation leads implant based on anatomical landmarks with standard surgical implantation technique.


Clinical Trial Description

The primary purpose of this study is to compare the therapeutic efficacy of the conventional, paresthesia mapping-based burst spinal cord stimulation (SCS) implantation strategy to a more novel, anatomic midline-based approach that has the potential to streamline the workflow associated with the SCS treatment continuum. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02986074
Study type Interventional
Source Abbott Medical Devices
Contact
Status Completed
Phase N/A
Start date November 2016
Completion date August 19, 2019

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