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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorTanta University

About this trial

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

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

Allergy to local anesthetics.

Infection at the injection site.

Coagulopathy or bleeding disorders.

Neuromuscular disorders.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Quadroiliac Plane Block

    Drug

    Patients will receive an ultrasound-guided Quadroiliac Plane Block (QIPB) using 20 mL of bupivacaine 0.25%.

  • Transmuscular quadratus lumborum block

    Drug

    Patients will receive ultrasound-guided quadratus lumborum block (QLB) (transmuscular approach) using 20 mL of 0.25% bupivacaine.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group QIPExperimental treatment 1 intervention
Group B: Group QLBExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Total morphine consumption

Rescue analgesia of morphine will be given as 3 mg bolus if the numeric rating scale (NRS) \> 3 to be repeated after 30 min if pain persists until the NRS \< 4.

Time frame
24 hours postoperatively

Secondary outcomes

1

Degree of pain

Each patient will be instructed about postoperative pain assessment with the numeric rating scale (NRS) score. NRS (0 represents "no pain" while 10 represents "the worst pain imaginable"). NRS will be assessed at post-anesthesia care unit (PACU), 2, 4, 6, 12, and 24 h postoperatively.

Time frame
24 hours postoperatively
2

Time to the 1st rescue analgesia

Time to the first request for rescue analgesia will be recorded from the end of block to first dose of morphine administrated.

Time frame
24 hours postoperatively
3

Time for ambulation

Time to ambulation: the time interval (in hours) from the end of surgery to the first successful mobilization of the patient, defined as the ability to stand and walk at least 3-5 steps with or without assistance.

Time frame
24 hours postoperatively
4

Length of hospital stay

Length of hospital stay will be recorded from admission till the discharge from hospital.

Time frame
Till the discharge from hospital (Up to 2 weeks)

Other outcomes

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