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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorFatih Sultan Mehmet Training and Research Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Refusal to participate in the study

Emergency surgery

Local infection or hematoma at the block application site

Previous surgery at the block application site

Trial population

Adult patients aged 18-65 years with ASA physical status I-III and body mass index \<35 kg/m² scheduled for elective posterior lumbar segmental instrumentation surgery under general anesthesia. All participants provide written informed consent prior to enrollment.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • QIPB

    Other intervention

    Quadro-Iliac Plane Block using local anesthetic.

  • LAI

    Other intervention

    The surgeon will perform local anesthetic infiltration (LAI) of the incision site.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: PCA + QIPB Group1 intervention
Group B: PCA + LAI Group1 intervention

Trial outcomes

Primary outcomes

1

Postoperative Pain Intensity

Postoperative pain intensity assessed using the Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates the worst imaginable pain.

Time frame
Within the first 24 hours after surgery

Secondary outcomes

1

Total Opioid Consumption

Total amount of tramadol consumption administered via intravenous patient-controlled analgesia during the first 24 hours postoperatively.

Time frame
Within the first 24 hours after surgery
2

Requirement for Rescue Analgesia

Need for additional rescue analgesic medication during the first 24 hours postoperatively.

Time frame
Within the first 24 hours after surgery
3

Postoperative Nausea and Vomiting

Incidence of postoperative nausea and vomiting during the first 24 hours after surgery.

Time frame
Within the first 24 hours after surgery
4

Patient Satisfaction With Pain Management

Patient satisfaction with postoperative pain management was assessed at 24 hours after surgery using a 5-point Likert Satisfaction Scale (range: 1-5), where 1 = "not satisfied at all," 2 = "not satisfied," 3 = "neutral," 4 = "satisfied," and 5 = "very satisfied," with higher scores indicating greater patient satisfaction.

Time frame
24 hours after surgery

Other outcomes

Sponsors and contacts

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