120
Participants
Start Date
August 15, 2022
Primary Completion Date
April 12, 2023
Study Completion Date
June 30, 2023
BioWave
The BioWave device is called BioWaveGO. It is a FDA 510(k) cleared high frequency sinusoidal neurostimulator
TENS
The TENS device is called Intensity 5000. It is a FDA 510(k) cleared TENS device
Center for Interventional Pain and Spine, Lancaster
Carolinas Pain Center, Huntersville
University of Wisconsin, Madison
Yale, New Haven
Lead Sponsor
Center For Interventional Pain and Spine
OTHER
Yale University
OTHER
University of Wisconsin, Madison
OTHER
BioWave Corporation
INDUSTRY