Comparison of Quadratus Lumborum and Combined Groin Nerve Blocks for Postoperative Analgesia After Open Inguinal Hernia Repair.

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorAl-Azhar University

About this trial

This double-blind randomized controlled trial aimes to compares two ultrasound-guided regional techniques-lateral quadratus lumborum block versus combined ilio-inguinal/ilio-hypogastric/genitofemoral (II-IH-GFN) block-for postoperative analgesia after elective unilateral open inguinal hernia repair under spinal anesthesia in adults.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 18-75 years.

ASA physical status I-III.

Scheduled for elective unilateral open inguinal hernia repair under standardized spinal anesthesia.

Able to understand and use the Visual Analogue Scale (VAS).

Disqualifiers

Allergy to local anesthetics.

Coagulopathy or current use of anticoagulants contraindicating peripheral nerve blocks.

Infection at the injection site.

Chronic opioid use (daily opioids >2 weeks) or chronic pain syndromes.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ultrasound-guided lateral quadratus lumborum block

    Procedure/Surgery

    Ultrasound-guided lateral quadratus lumborum block. Local anesthetic: 30 ml of (Ropivacaine 0.2%) is injected at the appropriate fascial level.

  • Combined ilio-inguinal/ilio-hypogastric/genitofemoral (II-IH-GFN) block

    Procedure/Surgery

    Ultrasound-guided ilio-inguinal and ilio-hypogastric block. Local anesthesia: 20 ml of 0.2% ropivacaine for ilio-inguinal and ilio-hypogastric block + 10 ml of 0.2% ropivacaine for genitofemoral anaesthesia, total injection volume = 30 ml.

Treatment groups

66 Participants
are divided into 2 treatment groups
Group A: Group 1 (Quadratus lumborum block)Active comparator 1 intervention
Group B: Group 2 ( Ilio-inguinal and ilio-hypogastric block)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Cumulative opioid consumption in the first 24 hours postoperatively

Measures the total amount of opioid analgesics (expressed as morphine milligram equivalents, MME) consumed during the first postoperative 24 hours. It reflects overall analgesic efficacy of the two block techniques.

Time frame
24 hours after surgery.

Secondary outcomes

1

Pain intensity (VAS pain scores at rest )

Assesses the level of postoperative pain at rest using the Visual Analogue Scale (VAS), where 0 = no pain and 10 = worst imaginable pain.

Time frame
24 hours postoperatively.
2

Pain intensity (VAS pain scores at movement)

Assesses the level of postoperative pain during movement using the Visual Analogue Scale (VAS), where 0 = no pain and 10 = worst imaginable pain.

Time frame
24 hours postoperatively.
3

Time to first analgesic request

Determines the duration of effective analgesia provided by each block, defined as the interval from completion of the block to the first patient request for additional analgesia.

Time frame
24 hours.
4

Proportion of patients requiring rescue opioid analgesia

Percentage of patients who required additional opioid analgesics beyond the planned postoperative regimen, indicating inadequate analgesia from the primary block.

Time frame
24 hours.

Other outcomes

Sponsors and contacts

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Al-Azhar University

Lead sponsor

Benha University

Collaborator

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