Clinical Trials Directory

Trials / Terminated

TerminatedNCT04588389

Comparison of Quadratus Lumborum Block Types

Comparison of Quadratus Lumborum Block With Medical Management for Pain Control After Lumbar Spine Fusion Surgery

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
9 (actual)
Sponsor
University of Massachusetts, Worcester · Academic / Other
Sex
All
Age
40 Years – 80 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine injection Location 1Ropivacaine .5% and lidocaine 1% to the area behind the muscle Quadratus Lumborum location 1
DRUGRopivacaine injection Location 2Ropivacaine .5% and lidocaine 1% to the area behind the muscle Quadratus Lumborum location 2
DRUGMultimodal Pharmacological Managementstandard of care multimodal pharmacological management

Timeline

Start date
2020-12-01
Primary completion
2021-05-14
Completion
2021-05-14
First posted
2020-10-19
Last updated
2025-07-28
Results posted
2025-07-28

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04588389. Inclusion in this directory is not an endorsement.