Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT07326774

Effect of Ultrasound-Guided Quadro-Iliac Plane Block on Postoperative Analgesia After Lumbar Spinal Surgery

Led by Fatih Sultan Mehmet Training and Research Hospital · Updated on 2026-02-23

60

Participants Needed

1

Research Sites

38 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective observational study aims to evaluate the effect of ultrasound-guided Quadro-Iliac Plane Block (QIPB) on postoperative analgesia in patients undergoing lumbar spinal surgery. Lumbar spinal procedures are commonly associated with significant postoperative pain, which may impair early mobilization and increase opioid consumption. In routine clinical practice, QIPB is increasingly used as part of multimodal analgesia to improve pain control and reduce opioid-related adverse effects. Adult patients scheduled for elective lumbar spinal surgery under general anesthesia will be followed according to routine clinical care. Postoperative analgesia will be managed with intravenous patient-controlled analgesia (PCA) using tramadol, with or without the addition of ultrasound-guided QIPB, based on the preference of the attending anesthesiologist. No intervention or treatment assignment will be performed by the investigators. Postoperative pain scores at rest and during movement, opioid consumption, need for rescue analgesics, incidence of nausea and vomiting, and patient satisfaction will be recorded during the first 24 hours after surgery. The findings of this study are expected to provide further clinical evidence regarding the effectiveness of QIPB as part of multimodal analgesia in lumbar spinal surgery.

CONDITIONS

Official Title

Effect of Ultrasound-Guided Quadro-Iliac Plane Block on Postoperative Analgesia After Lumbar Spinal Surgery

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged between 18 and 65 years
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Body mass index (BMI) <35 kg/m²
  • Scheduled for elective posterior lumbar spinal instrumentation surgery under general anesthesia
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study
  • Emergency surgery
  • Local infection or hematoma at the block application site
  • Previous surgery at the block application site
  • Presence of coagulopathy
  • Known allergy or toxicity to local anesthetics
  • History of hematological, renal, or hepatic disease, or advanced respiratory or cardiac failure
  • Chronic analgesic use, chronic alcohol consumption, or substance abuse
  • Inability to speak Turkish or presence of language/communication barriers

AI-Screening

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Trial Site Locations

Total: 1 location

1

Fatih Sultan Mehmet Training and Research Hospital

Istanbul, Istanbul, Turkey (Türkiye), 34752

Actively Recruiting

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Research Team

E

Elif Acar Deger, Dr.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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