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Trigger Point Injections Versus Lidocaine Patch for Myofascial Pain in the Emergency Department

Myofascial Trigger Point Pain Clinical Trial

Official title:
A Randomized Controlled Study Comparing Trigger Point Injections With 1% Lidocaine Versus 5% Lidocaine Patch for Myofascial Pain in the Emergency Department

Clinical Trial Summary

The aim of this trial is to investigate the efficacy of trigger point injections with 1% lidocaine in reducing myofascial back and neck pain in the Emergency Department compared to lidocaine patches 5%.

Clinical Trial Description

After being informed about the study and the potential risks and benefits, all patients will be randomized into either the trigger point injection group with 1% lidocaine, or the 5% lidocaine patch group. Pain scores will be recorded while in the emergency department, and we will have a 5 day follow-up phone call to assess efficacy. Patients who present to UCI Department of Emergency medicine will be screened and recruited prospectively, and information regarding this study will be available on clinicaltrials.gov as a method of recruitment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05151510
Study type Interventional
Source University of California, Irvine
Contact Jonathan B Lee, MD
Phone 9098963192
Email jonbryanlee@gmail.com
Status Recruiting
Phase Phase 4
Start date November 1, 2021
Completion date December 2024
View Details
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