Clinical Trial

Postoperative Pain Monitoring With ANI in Lumbar Spine Surgery

Study acronym: SPINE-ANI
Recruiting
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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.
Trial Details
NCT Number NCT07455565
Lead Sponsor Akdeniz University Hospital
Conditions Postoperative Pain, Lumbar Spine Surgery
Enrollment 100 participants
Start Date 2025-12-16
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-03-06