Postoperative Pain Monitoring With ANI in Lumbar Spine Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAkdeniz University Hospital

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

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators