Clinical Trial

Evaluating the Effectiveness of Postoperative Analgesic Methods in Thoracotomy Cases

Completed
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Summary
Effective control of severe post-thoracotomy pain is pivotal for minimizing pulmonary complications and enhancing patient comfort. This prospective, randomized, three-arm study compared the analgesic efficacy of ultrasound-guided bilateral erector spinae plane block (ESPB) and thoracic epidural analgesia (TEA) with conventional intravenous opioid-based care. Seventy-two ASA I-II patients aged 18-80 years undergoing elective thoracotomy were block-randomized to receive TEA, ESPB, or no regional intervention (control). All procedures were performed at the end of surgery before emergence from anesthesia. Pain intensity was assessed at 1, 2, 4, 6, 12, and 24 h postoperatively using the Visual Analog Scale (VAS). Additional outcomes included time to first rescue opioid, total tramadol consumption, time to modified Aldrete score (MAS) ≥ 9, patient satisfaction, and length of hospital stay.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-03-14.
Trial Details
NCT Number NCT07482449
Lead Sponsor Denizhan Acar
Conditions Thoracotomy Analgesia
Enrollment 72 participants
Start Date 2023-05-08
Primary Completion 2025-05-20 (estimated)
Study Completion 2026-02-12 (estimated)
Updated on ClinicalTrials.gov 2026-03-23