Quadro-Iliac Plane Block for Pain Control After Posterior Spinal Instrumentation Surgery

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-80
SponsorIstanbul Medipol University Hospital

About this trial

Posterior spinal instrumentation can cause significant postoperative pain due to extensive muscle dissection, manipulation of bone tissue, and implant placement. Providing optimal analgesia in the postoperative period is important for patients' functional recovery and early mobilization. Inadequate control of postoperative pain may delay recovery, increase the risk of opioid dependence, and lead to respiratory complications.

Although opioid analgesics are effective in reducing pain during the postoperative period, they are associated with side effects such as nausea, vomiting, respiratory depression, and the risk of dependence. Therefore, the use of non-opioid analgesic approaches is important for patient safety and comfort. For these reasons, regional analgesia techniques such as the modified thoracolumbar interfascial plane (TLIP) block and the erector spinae plane (ESP) block have recently become increasingly popular for postoperative pain control. The quadro-iliac plane block is a novel technique that targets the attachment area of the posterior surface of the quadratus lumborum muscle on the inner surface of the iliac crest. In this block, the spread of local anesthetic along the fascial planes surrounding the quadratus lumborum muscle may provide an anatomical mechanism contributing to analgesia of the lumbosacral, paraspinal, lower abdominal, and gluteal regions. However, as the quadro-iliac plane block is a new technique, there are not yet sufficient studies on this topic in the literature.

The primary objective of our study is to evaluate the effect of ultrasound-guided quadro-iliac plane block (QIPB) on postoperative opioid consumption after posterior spinal instrumentation. The secondary objectives are to compare opioid-related side effects, such as nausea, vomiting, and respiratory depression, as well as postoperative NRS (Numeric Rating Scale) pain scores between the groups.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Posterior spinal instrumentation patients

Disqualifiers

Contraindications for regional analgesia

Allergies for local anesthetics

Trial design

Design model

Parallel

Treatments tested in this trial

  • Fentanyl (IV)

    Drug

    All patients will have an IV PCA with fentanyl.The PCA settings will consist of a 10-µg fentanyl bolus dose with a 10-minute lockout interval.

  • Meperidine

    Drug

    If the patient's NRS is 4 or more even though 1 gr IV paracetamol and IV PCA, meperidine 0.5 mg/kg w'll be administered as rescue analgesic

  • Paracetamol (acetaminophen)

    Drug

    An order for intravenous paracetamol 1 g every 8 hours will be placed for all patients.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Quadro-iliac block groupActive comparator 3 interventions
Group B: Wound infiltration GroupOther 3 interventions

Trial outcomes

Primary outcomes

1

The effect of ultrasound-guided quadro-iliac plane block (QIPB) on postoperative opioid consumption f

The primary objective of this study is to evaluate the effect of ultrasound-guided quadro-iliac plane block (QIPB) on postoperative opioid consumption following posterior spinal instrumentation surgery.

Time frame
Postoperative 24 hours

Secondary outcomes

1

NRS of patients

Time frame
Postoperative 24 hours
2

Opioid related adverse effects

Time frame
Postoperative 24 hours

Other outcomes

Sponsors and contacts

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