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NCT04588389

Comparison of Quadratus Lumborum Block Types

Terminated Phase 3 Results posted Last updated 28 July 2025
What this trial tests

Phase 3 trial testing Ropivacaine injection Location 1 in Pain in 9 participants. Terminated before completion.

Timeline
1 December 2020
Primary endpoint
14 May 2021
14 May 2021

Quick facts

Lead sponsorUniversity of Massachusetts, Worcester
PhasePhase 3
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment9
Start date1 December 2020
Primary completion14 May 2021
Estimated completion14 May 2021
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Massachusetts, Worcester

Who can join

Adults 40 to 80, any sex, with Pain or Opioid Use. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Opioid Consumption Primary · 12 hours

Dose of the opioids consumed

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II307.5 – 37.5
Group 3 Standard of Care + Quadratus Lumborum Block III17.57.5 – 22.5
Opioid Consumption Primary · 24 hours

Dose of the opioids consumed

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II317.5 – 56.25
Group 3 Standard of Care + Quadratus Lumborum Block III2015 – 37.5
Opioid Consumption Primary · 36 hours

Dose of the opioids consumed

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II35.62515 – 52.5
Group 3 Standard of Care + Quadratus Lumborum Block III207.5 – 30
Opioid Consumption Primary · 48 hours

Dose of the opioids consumed

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II31.87515 – 45
Group 3 Standard of Care + Quadratus Lumborum Block III2515 – 30
Pain Scale Secondary · 0 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II85 – 10
Group 3 Standard of Care + Quadratus Lumborum Block III3.670 – 7
Pain Scale Secondary · 1 Hour

Numerical Pain Scale Rating of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II4.753 – 8
Group 3 Standard of Care + Quadratus Lumborum Block III20 – 4
Pain Scale Secondary · 6 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II5.253 – 8
Group 3 Standard of Care + Quadratus Lumborum Block III2.330 – 4
Pain Scale Secondary · 12 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II5.254 – 8
Group 3 Standard of Care + Quadratus Lumborum Block III5.334 – 8
Pain Scale Secondary · 18 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II64 – 9
Group 3 Standard of Care + Quadratus Lumborum Block III5.333 – 8
Pain Scale Secondary · 24 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II5.754 – 7
Group 3 Standard of Care + Quadratus Lumborum Block III4.673 – 6
Pain Scale Secondary · 30 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II4.750 – 8
Group 3 Standard of Care + Quadratus Lumborum Block III2.30 – 5
Pain Scale Secondary · 36 Hours

Numerical Pain Scale Rating, likert scale of 0-10 with a 0 indicating absence of pain and 10 indicating worst pain imaginable.

GroupValue95% CI
Group 2 Standard of Care + Quadratus Lumborum Block II6.254 – 9
Group 3 Standard of Care + Quadratus Lumborum Block III6.334 – 10

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pain

Currently open trials in the same condition.

Other University of Massachusetts, Worcester trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing