SPS Block vs. Surgical Intercostal Block for Chronic Pain After Thoracoscopic Surgery
Condition(s) studied
Investigational drug(s) / intervention(s)
SPS block: 30 mL of 0.25% Bupivacaine will be injected into the plane between the Serratus Posterior Superior muscle and the intercostal muscles at the scapular level.
Surgical Intercostal Blockade.: At the end of the operation, the surgeon will perform an injection of a total of 30 mL of 0.25% Bupivacaine into three intercostal nerves above and below the incision site under direct thoracoscopic visualization.
Study 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).
Eligibility
Primary outcome measure(s)
- Incidence and severity of Chronic Post-Thoracotomy Pain (CPTP) — Incidence and severity of Chronic Post-Thoracotomy Pain (CPTP) at 3, 6, and 12 months post-surgery.
The primary aim is to compare incidence and severity of Chronic Post-Thoracotomy Pain with McGill Pain Questionnaire (MPQ).
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Istanbul Medipol University Hospital | Istanbul | Bagcilar | Recruiting |
More Medipol University trials in Turkey
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07436806 on ClinicalTrials.gov ↗ ← All trials in Turkey