Deep iliacus plane block vs transmuscular quadratus lumborum block for hip surgery pain relief
Official title: Deep Iliacus Plane Block Versus Transmuscular Quadratus Lumborum Block for Postoperative Analgesia After Total Hip Arthroplasty: A Randomized Clinical Trial
Run by Tanta University · NCT07798830 · Data updated 2026-11-12
This study tests whether the deep iliacus plane block provides better pain relief and recovery than the transmuscular quadratus lumborum block after total hip replacement.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Status | Recruiting |
| Started | September 1, 2026 |
| Main results expected | March 1, 2027 |
| Study ends | March 1, 2027 |
| Registry record updated | September 2, 2026 |
| Trial ID | NCT07798830 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years and older undergoing elective unilateral THA under spinal anesthesia, ASA I–III, without contraindications to regional anesthesia or chronic opioid use.
✕Probably not a fit
Patients with contraindications to regional anesthesia, chronic opioid use, or higher BMI (>40 kg/m²) may not benefit or could be at greater risk.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial compares two ultrasound-guided regional anesthesia techniques, DIPB and QLB, in adults undergoing elective unilateral total hip arthroplasty under spinal anesthesia. It looks at analgesic effectiveness, opioid use, preserved motor function, and quality of recovery. Participants are ASA I–III adults aged 18 or older, without contraindications to regional anesthesia or chronic opioid use. The study is conducted at Tanta University, sponsored by Tanta University. The aim is to determine which block offers superior postoperative pain control with favorable recovery profiles.
Why it matters
Potential benefit: If successful, the DIPB could offer superior pain control with similar or better recovery and potentially lower opioid needs.
How similar studies have gone: Regional blocks for hip surgery have shown benefits, but direct comparison between DIPB and QLB is relatively novel and data are evolving.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years. * Both sexes. * American Society of Anesthesiologists (ASA) physical status I-III. * Scheduled for elective unilateral total hip arthroplasty (THA) under spinal anesthesia. Exclusion Criteria: * Known allergy to local anesthetics or study medications. * Coagulopathy or anticoagulant therapy contraindicating regional anesthesia. * Infection at the site of injection. * Pre-existing neurological deficits affecting the lower limbs. * Chronic opioid use or opioid dependence. * Severe hepatic, renal, respiratory, or cardiac disease. * Body mass index (BMI) \> 40 kg/m². * Contraindications to spinal anesthesia.
Where it's running
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Tanta University
Tanta, El-Gharbia, Egypt Recruiting
Study contacts
- Study coordinator: Mohammed S Elsharkawy, MD
- Email: mselsharkawy@med.tanta.edu.eg
- Phone: 00201148207870
Similar studies
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This study tests whether the Quadroiliac Plane Block provides better postoperative pain relief and lower opioid use than the transmuscular quadratus lumborum block after total hip arthroplasty conducted under spinal anesthesia.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.