Ultrasound-Guided Erector Spinae Plane Block in Major Spinal Surgery

Conditions: Perioperative Bleeding, Opioid Consumption, Erector Spinae Plane Block, Spinal Stabilization

Sex: All

Ages: 18 Years – 90 Years

Healthy volunteers: No

Phase: NA

Enrollment: 120

Sponsor: Diskapi Yildirim Beyazit Education and Research Hospital

Summary

This study aims to evaluate the effects of ultrasound-guided bilateral erector spinae plane block on intraoperative pain control and bleeding in patients undergoing major spinal surgery. Participants will be randomly assigned to two groups: one group will receive the Erector Spinae Plane block, while the other group will receive standard pain management. Primary outcomes include postoperative pain levels and intraoperative blood loss. This study seeks to determine whether the Erector Spinae Plane Block technique positively contributes to patient recovery and reduces bleeding complications.

Eligibility Criteria

Inclusion Criteria: * Patients aged 18 years or older Scheduled for elective spinal stabilization surgery American Society of Anesthesiologists (ASA) physical status I-III Provided written informed consent Exclusion Criteria: Coagulopathy or current anticoagulant therapy Anatomical barrier or infection at the Erector Spinae Plane Block site Known allergy to local anesthetics or opioids \-

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07101198). StuddyBuddy aggregates publicly available trial information.