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Recruiting NCT07815145

NCT07815145 Quadroiliac Plane Block Versus Transmuscular Quadratus Lumborum Block for Postoperative Analgesia After Total Hip Arthroplasty

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Clinical Trial Summary
NCT ID NCT07815145
Status Recruiting
Phase —
Sponsor Tanta University
Condition Quadroiliac Plane Block
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2026-09-12
Primary Completion 2027-02-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
Quadroiliac Plane BlockTransmuscular quadratus lumborum block

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2026-09-12 with a primary completion date of 2027-02-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to evaluate and compare the postoperative analgesic efficacy, opioid consumption, motor function preservation, and quality of recovery of ultrasound-guided Quadroiliac Plane Block (QIPB) versus transmuscular quadratus lumborum block (QLB) in patients undergoing THA under spinal anesthesia.

Eligibility Criteria

Inclusion Criteria: * Age 18-75 years. * Both sexes. * American Society of Anesthesiologists (ASA) classification I-III. * Scheduled for elective primary unilateral total hip arthroplasty under spinal anesthesia. Exclusion Criteria: * Allergy to local anesthetics. * Infection at the injection site. * Coagulopathy or bleeding disorders. * Neuromuscular disorders. * Chronic opioid use or dependence. * Body mass index (BMI) \> 40 kg/m². * Severe cardiac, hepatic, renal, or respiratory dysfunction. * Contraindication to regional anesthesia.

Contact & Investigator

Central Contact

Mohammed S Elsharkawy, MD

✉ mselsharkawy@med.tanta.edu.eg

📞 00201148207870

Frequently Asked Questions

Who can join the NCT07815145 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Quadroiliac Plane Block. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07815145 currently recruiting?

Yes, NCT07815145 is actively recruiting participants. Contact the research team at mselsharkawy@med.tanta.edu.eg for enrollment information.

Where is the NCT07815145 trial being conducted?

This trial is being conducted at Tanta, Egypt.

Who is sponsoring the NCT07815145 clinical trial?

NCT07815145 is sponsored by Tanta University. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology