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Clinical Trial Summary

Prospective, single arm, open label, multi-center study to evaluated the effectiveness of intraosseous basivertebral nerve radiofrequency ablation using the Intracept System.


Clinical Trial Description

This is a prospective, open-label, single-arm study of patients diagnosed with vertebrogenic low back pain for a minimum of 6 months with conservative care. Participants will receive the Intracept System procedure to ablate the basivertebral nerve within the vertebral body. Treatment is performed on all vertebral bodies with Modic type 1 or type 2 changes on MRI from L3-S1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03266107
Study type Interventional
Source Relievant Medsystems, Inc.
Contact
Status Completed
Phase N/A
Start date February 14, 2018
Completion date February 17, 2020

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