Ireland
--:--IST
Recruiting Not applicable

Quadro-Iliac Plane Block for Analgesia After Lumbar Microdiscectomy

NCT07695987 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-07-10
Last updated
2026-07-30

Condition(s) studied

Pain Management

Investigational drug(s) / intervention(s)

Ultrasound-Guided Quadro-Iliac Plane BlockLocal Infiltration Analgesia (LIA)

Ultrasound-Guided Quadro-Iliac Plane Block: Bilateral ultrasound-guided quadro-iliac plane block will be performed before emergence from general anesthesia in the prone position. After visualization of the quadratus lumborum muscle and iliac crest at the L3 level, 30 mL of 0.167% bupivacaine will be injected into the interfascial plane on each side. All participants will receive postoperative fentanyl-based patient-controlled analgesia.

Local Infiltration Analgesia (LIA): Local infiltration analgesia will be performed by the surgeon before the end of surgery. A total dose of 50 mg of 0.25% bupivacaine will be infiltrated into the subcutaneous tissue. All participants will receive postoperative fentanyl-based patient-controlled analgesia.

Study summary

This study will evaluate whether ultrasound-guided quadro-iliac plane block provides better postoperative pain control than local infiltration analgesia in patients undergoing single-level lumbar microdiscectomy.

Adult patients scheduled for elective single-level lumbar microdiscectomy will be randomly assigned to receive either bilateral quadro-iliac plane block plus patient-controlled analgesia or local infiltration analgesia plus patient-controlled analgesia. The main outcome of the study will be total fentanyl consumption during the first 24 hours after surgery. Pain scores, need for rescue analgesia, opioid-related side effects, patient satisfaction, and recovery quality will also be evaluated.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 to 75 years * American Society of Anesthesiologists physical status I to III * Scheduled for elective single-level lumbar microdiscectomy, such as L4-L5 or L5-S1 disc herniation * Planned surgery under general anesthesia * Able to provide written informed consent Exclusion Criteria: * Allergy or hypersensitivity to local anesthetics * Coagulopathy or active anticoagulant use * Infection, scar tissue, or skin lesion at the injection site * Pregnancy or breastfeeding * Chronic pain syndrome or regular opioid use * American Society of Anesthesiologists physical status IV or higher * Planned surgery for two or more levels of disc herniation

Primary outcome measure(s)

  • Total Fentanyl Consumption During the First 24 Hours After Surgery — Postoperative 0-24 hours
    Total postoperative fentanyl consumption administered via patient-controlled analgesia will be recorded during the first 24 hours after surgery.

Trial sites (1)

FacilityCityRegionStatus
Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital Istanbul Istanbul Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07695987 on ClinicalTrials.gov ↗ ← All trials in Turkey