Clinical Trial

Serratus Posterior Superior Intercostal Plane Block Versus Intrathecal Morphine in VATS

Recruiting
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Record status
This record was last updated August 10, 2026 (before its estimated August 15, 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to compare the analgesic effects of the serratus posterior superior intercostal plane block and intrathecal morphine in patients undergoing video-assisted thoracoscopic surgery. This is a prospective, randomized, controlled, single-center clinical trial including adult patients undergoing elective thoracoscopic surgery. Participants will be randomly assigned to receive either a serratus posterior superior intercostal plane block or intrathecal morphine before general anesthesia. The primary outcome is cumulative opioid consumption during the first 24 postoperative hours, expressed as intravenous morphine milligram equivalents. Secondary outcomes include pain scores, time to first analgesic request, quality of recovery, and postoperative complications. The study aims to determine whether these two techniques differ in their effectiveness for postoperative pain management.
Protocol Amendment History 2 changes
critical Primary endpoint(s) modified 2026-07-31
critical Recruitment opened 2026-05-05
Trial Details
NCT Number NCT07540104
Lead Sponsor Ondokuz Mayıs University
Conditions Thoracic Anesthesia, Postoperative Pain, Video Assisted Thoracic Surgery (VATS)
Enrollment 60 participants
Start Date 2026-04-15
Primary Completion 2026-08-15 (estimated)
Study Completion 2026-09-15 (estimated)
Updated on ClinicalTrials.gov 2026-08-10