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Bilateral Erector Spinae Plane Block Versus Bilateral Quadratus Lumborum Plane Block for Postoperative Anaelgesia After Lumbar Spine Surgery

Bilateral Erector Spinae Plane Block Versus Bilateral Quadratus Lumborum Plane Block for Postoperative Anaelgesia After Lumbar Spine Surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07517822
Enrollment
40
Registered
2026-04-08
Start date
2025-12-01
Completion date
2026-07-01
Last updated
2026-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaesthesia

Brief summary

The aim of this study is to compare postoperative analgesia and duration for each block performance plus complications after surgery in lumbar spine fixation.

Interventions

PROCEDUREUltrasound-guided quadratus lumborum block (QLB)

And ultrasound guided QLB block with transmuscular approach was performed using 0.5 ml/kg 0.25% bupivacaine to the patients in QLB group

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 18 and 65 years. * American Society of Anesthesiologists (ASA) physical status I to II. * Body mass index (BMI) less than 35 kg/m2.

Exclusion criteria

* Revision surgery. * More than three levels surgery. * Abnormal state of blood coagulation. * Chronic opioid consumption. * Local infection at the injection site). * Allergy to any involved medications. * Taking opioids within the past two weeks prior to surgery. * Time of surgery more than 4 hours.

Design outcomes

Primary

MeasureTime frameDescription
Comparison between postoperative analgesia of QLB and ESPB after lumbar spine surgery via VAS score measurementVAS Score will be used to assess pain or discomfort in postoperative at 2, 4, 6, 12, 24 hoursThe Visual Analog Scale (VAS) is used to assess pain intensity. It consists of a 10 cm line where 0 indicates "no pain" and 10 indicates "the worst possible pain." Higher scores indicate greater pain intensity.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 9, 2026