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Clinical Trial Summary

This study is designed to evaluate the clinical utility of a known intraoperative neuromonitoring modality (SSEP) using saphenous nerve as the site of stimulation to identify changes to the lumbar nerves which may be at risk during the lateral lumbar interbody fusion (LLIF) procedure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05648474
Study type Observational
Source Alphatec Spine, Inc.
Contact
Status Recruiting
Phase
Start date July 13, 2022
Completion date December 31, 2025

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