drugset / Trial / NCT07455565

Postoperative Pain Monitoring With ANI in Lumbar Spine Surgery

NCT07455565 ↗

Recruiting 100 enrolled Akdeniz University Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims to compare two different pain management methods in patients undergoing elective lumbar spine surgery. Patients are randomly assigned to receive either an ultrasound-guided erector spinae plane block (ESPB) or intravenous multimodal analgesia. Postoperative pain will be assessed using both clinical pain scores and the Analgesia Nociception Index (ANI), a non-invasive monitoring system that evaluates pain-related responses based on heart rate variability. The goal of this study is to determine which method provides better postoperative pain control.

Timeline

Start
2025-12-16
Primary completion
2026-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acetaminophen Small molecule 1 g Intravenous
Comparator Dexamethasone Small molecule 8 mg Intravenous
Comparator Ketamine Small molecule 0.3 mg/kg Intravenous
Comparator Morphine Other / unclassified 0.1 mg/kg Intravenous

Indications

No indication recorded.