Clinical Trial

SPS Block vs. Surgical Intercostal Block for Chronic Pain After Thoracoscopic Surgery

Recruiting
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Summary
This study aims to evaluate the efficacy of ultrasound-guided Serratus Posterior Superior (SPS) block compared to surgeon-administered intercostal blockade in preventing chronic pain at 3, 6, and 12 months following Video-Assisted Thoracoscopic Surgery (VATS).
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-02-23.
Status change: Not Yet Recruiting → Recruiting 2026-03-06
Trial Details
NCT Number NCT07436806
Lead Sponsor Medipol University
Conditions Chronic Post-thoracotomy Pain, Neuropathic Pain, Postoperative Pain, Acute
Enrollment 40 participants
Start Date 2026-03-01
Primary Completion 2026-11-20 (estimated)
Study Completion 2026-12-10 (estimated)
Updated on ClinicalTrials.gov 2026-03-10