Quadro-Iliac Plane Block for Analgesia After Lumbar Microdiscectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorKanuni Sultan Suleyman Training and Research Hospital

About this trial

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 criteria

Qualifiers

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

Disqualifiers

Allergy or hypersensitivity to local anesthetics

Coagulopathy or active anticoagulant use

Infection, scar tissue, or skin lesion at the injection site

Pregnancy or breastfeeding

Trial design

Treatments tested in this trial

  • Ultrasound-Guided Quadro-Iliac Plane Block
  • Local Infiltration Analgesia (LIA)

Treatment groups

60 Participants
are divided into 2 treatment groups