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Serratus Posterior Superior Intercostal Plane Block Versus Intrathecal Morphine in VATS

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Trial completed
    • Eligibility criteria expanded, about 16 words
    • Secondary endpoints: details revised at 5 of 16 entries
    • Site details revised
  2. Primary completion date: Sep 1, 2026 to Aug 15, 2026
    • Study completion date: Sep 30, 2026 to Sep 15, 2026
    v4
  3. Primary endpoint(s) modified
    • Primary completion date: Sep 15, 2026 to Sep 1, 2026
    • Eligibility criteria expanded, about 12 words
    • Secondary endpoints: 14 to 16
    v3
  4. Recruitment openedv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07540104
Lead Sponsor Ondokuz Mayıs University
Conditions
(from sponsor)		 Thoracic Anesthesia, Postoperative Pain, Video Assisted Thoracic Surgery (VATS)
Related terms Agnosia, Postoperative Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov