Clinical trial Recruiting at 1 site Interventional Ages 18 and up

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.

More Postoperative Analgesia trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment80 (estimated)
SponsorTanta University
Academic / other
Locations1 site (Tanta, El-Gharbia)
StatusRecruiting
StartedSeptember 1, 2026
Main results expectedMarch 1, 2027
Study endsMarch 1, 2027
Registry record updatedSeptember 2, 2026
Trial IDNCT07798830 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

  • Tanta University
    Tanta, El-Gharbia, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.