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Clinical Trial Summary

This study is a prospective, single-arm, open label, single center to confirm the effectiveness and safety of an ultra-high frequency (500 KHz) spinal cord stimulation in patients with chronic back pain or lower limb pain.


Clinical Trial Description

This study is a prospective, single-arm, open label, single center to confirm the effectiveness and safety of an ultra-high frequency (500 KHz) spinal cord stimulation in patients with chronic back pain or lower limb pain. The trial length is 14 days. Patients will be given ultrahigh frequency pulse stimulation, up to 3 times in every 24 hours, and VAS will be obtained at least once a day. Compared to previous study conducted last year, patient can now have two lead implant sites for different pain locations. The electrode implantation site will be epidural space instead of Dorsal Root Ganglion (DRG). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03543085
Study type Interventional
Source GiMer Medical
Contact Yu-Kai Cheng, M.D.
Phone +886 4 2205 2121
Email master3743@gmail.com
Status Recruiting
Phase N/A
Start date April 12, 2018
Completion date December 31, 2018

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