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NOT YET RECRUITING
NCT07878936
NA

Quadro-Iliac Plane Block for Postoperative Analgesia in Laparoscopic Inguinal Hernia Repair

Sponsor: Marmara University Pendik Training and Research Hospital

View on ClinicalTrials.gov

Summary

The goal of this randomized controlled trial is to learn whether an ultrasound-guided quadro-iliac plane block (QIPB) reduces opioid use and pain after laparoscopic inguinal hernia repair in adults aged 18-65 years. The main question it aims to answer is: does QIPB reduce total tramadol consumption during the first 24 postoperative hours? Researchers will compare patients who receive QIPB under general anesthesia with patients who receive no block. All participants will receive the same general anesthesia, multimodal analgesia and intravenous tramadol patient-controlled analgesia (PCA). Pain scores, PCA use, quality of recovery (QoR-15), nausea and vomiting, and time to discharge will be recorded during the first 24 hours.

Official title: Comparison of Postoperative Opioid Requirement and Pain Scores in Patients With and Without Quadro-Iliac Plane Block Undergoing Laparoscopic Inguinal Hernia Repair: A Prospective Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

64

Start Date

2026-10-15

Completion Date

2027-10-15

Last Updated

2026-10-16

Healthy Volunteers

No

Interventions

PROCEDURE

Quadro-iliac plane block

With the patient in the lateral position, a low-frequency convex probe is placed parasagittally at the attachment of the quadratus lumborum to the iliac crest. Using an in-plane approach with a 100-mm block needle, position is confirmed with 5 mL saline, followed by 40 mL of 0.25% bupivacaine.