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Clinical Trial Summary

The purpose of the study is to investigate the differences in post-procedural pain scores and narcotic use among patients who receive a Superior Hypogastric Nerve Block (SHNB) with and without corticosteroid performed as part of the Uterine Artery Embolization (UAE) procedure.


Clinical Trial Description

Investigators will enroll a total of 28 women undergoing the UAE procedure with 14 subjects in each study arm. This investigation is a single blind randomized control trial investigating the post-procedural analgesic effect of adding a corticosteroid (Triamcinolone) as an adjuvant to a SHNB that contains bupivacaine for patients undergoing UAE, compared to patients undergoing nerve block for pain control following UAE with local anesthetic only. Before and after the procedure, patients will be asked to complete online surveys in order to record their pain score (measured on the Visual Analog Pain Scale), opioid and other pain medication use, and other symptoms, such as nausea. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04126824
Study type Interventional
Source University of California, Los Angeles
Contact Tammy L Floore
Phone 310-794-9202
Email tfloore@mednet.ucla.edu
Status Recruiting
Phase Early Phase 1
Start date November 5, 2019
Completion date February 2025

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