About this trial
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.
Eligibility criteria
Qualifiers
Age between 18 and 65 years
ASA physical status I-II
Scheduled for elective lumbar spine surgery
Ability to provide informed consent
Disqualifiers
Known allergy to study medications
Coagulation disorders
Infection at the block site
Severe cardiovascular disease
Trial design
Treatments tested in this trial
- Erector Spinae Plane Block
- Intravenous Multimodal Analgesia