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Clinical Trial Summary

This is a prospective, sham-controlled, randomized, single-blinded, multi-center study comparing two different modes of the NexWave device, transcutaneous electrical nerve stimulation (TENS) and interferential current (IFC), with an identical non-functioning NexWave sham device or self-defined standard of care for improvement of pain intensity of non-specific CLBP.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05972889
Study type Interventional
Source Zynex Medical, Inc.
Contact Kristin Andrud, PhD
Phone (800) 495-6670
Email kandrud@zynex.com
Status Recruiting
Phase N/A
Start date November 2, 2023
Completion date August 30, 2024

See also
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