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Clinical Trial Summary

Objective of study is to evaluate the procedural success rate, clinical effectiveness, and heath-economic profile using the Intercept Intraosseous Nerve Ablation System in adult subjects with chronic low back pain in the post-market setting


Clinical Trial Description

This is a prospective, open-label, single-arm, single-center study. There is no randomization or blinding. Subjects will receive the Intercept System procedure to treat one or two motion segments at L3/L4, L4/L5, or L5/S1 as identified by Modic Type 1 or 2 changes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03630133
Study type Interventional
Source Relievant Medsystems, Inc.
Contact
Status Withdrawn
Phase N/A
Start date May 8, 2018
Completion date February 29, 2020

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