Comparing Postoperative Pain Relief Using Quadratus Lumborum and Transversalis Fascia Blocks in Elective Inguinal Hernia Surgery
Led by Gaziosmanpasa Research and Education Hospital · Updated on 2026-07-07
60
Participants Needed
1
Research Sites
1 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are comparing the pain relief effects after surgery of two nerve block techniques the Transversalis Fascia Plane Block and the anterior Quadratus Lumborum Block. This study focuses on patients undergoing elective open inguinal hernia surgeries under spinal anesthesia. The goal is to assess which block delays the need for additional pain medication more effectively and improves postoperative comfort while reducing opioid side effects.
Participants receive either the anterior Quadratus Lumborum Block or the Transversalis Fascia Block applied under ultrasound guidance after surgery while in a lateral position. Both blocks involve injecting 20 mL of 0.25% bupivacaine near specific muscles to block nerve signals. All patients have spinal anesthesia during surgery and receive paracetamol after the procedure. Pain scores, analgesic use, and side effects like nausea are monitored for 24 hours.
During the study, patients are followed up at 2, 4, 8, 12, and 24 hours after surgery to measure pain levels using the Numeric Rating Scale and to record the time until first rescue pain medication is needed. Total opioid consumption and any postoperative side effects are tracked. Patients are monitored for 30 minutes after block administration, and rescue analgesics are provided if pain exceeds a certain level. The study aims to improve postoperative pain management and reduce opioid use after inguinal hernia surgery.
CONDITIONS
Brief Title
Analgesic Efficacy of Quadratus Lumborum vs. Transversalis Fascia Block in Inguinal Hernia Surgery
Research Team
S
serpil Sehirlioglu, MD
D
DÖNDÜ GENÇ MORALAR, MD
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American Society of Anesthesiologists (ASA) Classification 1 or 2
Scheduled for elective open inguinal hernia surgery
You will not qualify if you...
Allergy to local anesthetics
Infection at the procedure site
Body mass index over 35 kg/m²
Bleeding disorders or use of anticoagulants
Chronic use of analgesics or opioids
Mental or psychiatric disorders
ASA Classification 3 or 4, including severe COPD, history of cerebrovascular events, liver or kidney disease
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Block Application
Duration - Immediate postoperative period
After surgery, participants receive either the anterior Quadratus Lumborum Block or the Transversalis Fascia Block under ultrasound guidance while positioned on their side. They are monitored for 30 minutes after the block.
1 visit in block room
Postoperative Follow-up
Duration - 24 hours after surgery
Participants are assessed at 2, 4, 8, 12, and 24 hours after surgery for pain levels, rescue analgesic needs, side effects, and total pain medication use.
5 visits during 24 hours
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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Published Research Related To This Trial
A Prospective, randomized comparative study between ultrasound-guided posterior quadratus lumborum block and ultrasound-guided ilioinguinal/iliohypogastric nerve block for pediatric inguinal herniotomy.
Preemptive analgesic efficacy of ultrasound-guided transversalis fascia plane block in children undergoing inguinal herniorrhaphy: a randomized, double-blind, controlled study.
Ibrahim Abdelbaser, Nabil A Mageed, El-Sayed M El-Emam...
Ultrasound-guided quadratus lumborum block for postoperative pain control in patients undergoing unilateral inguinal hernia repair, a comparative study between two approaches.