Pain Clinical Trial - Comparison of Quadratus Lumborum Block Types

Status Recruiting

Clinical Trial Summary

This study will compare the quality of analgesia and reduction of opioid use, between standard of care and two groups of local anesthetic blocks in different location in the quadratus lumborum plane, for postoperative pain control after lumbar spinal fusion and if it reduces opioid consumption.

Clinical Trial Description

This study is a pilot study as part of planning for a larger randomized controlled trial. The study plans to enroll a total of 30 patients, with 10 patients randomly assigned in each group of the study. Group I will receive the standard of care multimodal pharmacological management. Group II will receive standard of care multimodal pharmacological management plus the Quadratus Lumborum II local anesthetic block. Group III will receive standard of care multimodal pharmacological management plus the Quadratus Lumborum III local anesthetic block. Measurements of opioid use, pain, and side effects will be recorded for each patient. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04588389
Study type	Interventional
Source	University of Massachusetts, Worcester
Contact	Ryan M DeWolf, MS
Phone	9783021857
Email	ryan.dewolf@umassmed.edu
Status	Recruiting
Phase	Phase 3
Start date	December 1, 2020
Completion date	December 31, 2022

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