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Basivertebral Nerve Block During Vertebral Augmentation: An Alternative Approach to Intraprocedural Pain Management

Vertebral Fracture Clinical Trial

Official title:
Basivertebral Nerve Block Performed in Conjunction With Vertebral Augmentation for Anesthesia

Clinical Trial Summary

The goal of this study is to assess the efficacy of lidocaine basivertebral nerve block as intraprocedural anesthesia during vertebral augmentation procedures.

Clinical Trial Description

Vertebral compression fractures secondary to osteoporosis can be treated with vertebral augmentation. Since intraprocedural pain is common during vertebral body endplate manipulation, these procedures are often carried out using conscious sedation or general anesthesia. Research has shown that the vertebral endplates are innervated by the basivertebral nerve, which has been successfully targeted via radiofrequency ablation to treat chronic vertebrogenic lower back pain. With this physiology in mind, the investigators will attempt to treated participants with vertebral compression using lidocaine-induced intraosseous basivertebral nerve block as the primary intraprocedural analgesia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04774029
Study type Interventional
Source Northwell Health
Contact
Status Completed
Phase Early Phase 1
Start date January 10, 2020
Completion date May 1, 2020
View Details
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