RecruitingNot ApplicableNCT07606794

Supra-Iliac Anterior Quadratus Lumborum Block and Pericapsular Nerve Group (PENG) Block for Analgesia After Total Hip Arthroplasty

A Randomized Clinical Non-Inferiority Trial Comparing Supra-Iliac Anterior Quadratus Lumborum Block and Pericapsular Nerve Group (PENG) Block for Analgesia After Total Hip Arthroplasty

Sponsor

Tanta University

Enrollment

50 participants

Start Date

May 23, 2026

Study Type

INTERVENTIONAL

Conditions

Analgesia Total Hip Arthroplasty Pericapsular Nerve Group Block Supra-Iliac Anterior Quadratus Lumborum Block

Summary

This study aims to compare the analgesic efficacy of supra-iliac anterior quadratus lumborum block (SA-QLB) and pericapsular nerve group (PENG) block in patients undergoing total hip arthroplasty (THA).

Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Pericapsular nerve group block and Supra-iliac anterior quadratus lumborum block for people with analgesia, pericapsular nerve group block, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 75 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERSupra-iliac anterior quadratus lumborum block

Patients will receive a supra-iliac anterior quadratus lumborum block (SA-QLB) using 20mL of bupivacaine 0.25%.

OTHERPericapsular nerve group block

Patients will receive an ultrasound-guided pericapsular nerve group (PENG) block using 20mL of bupivacaine 0.25%.

Locations(1)

Tanta University

Tanta, El-Gharbia, Egypt

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NCT07606794

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