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

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Mar 10, 2026 to Mar 1, 2026 · Site details revisedv2 Show 2 more changesShow less
    • Start date changed from estimate of Mar 10, 2026 to Mar 1, 2026
    • Site details revised
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 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).
Trial Details
NCT Number NCT07436806
Lead Sponsor Medipol University
Conditions Chronic Post-thoracotomy Pain, Neuropathic Pain, Postoperative Pain, Acute
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov