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Study identifier: NCT07436806 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Chronic Post-thoracotomy Pain · Neuropathic Pain · Postoperative Pain, Acute  ·  Sponsor: Medipol University

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Bahadir Ciftci, Assoc Prof, MD  ·  +905343736865  ·  bciftci@medipol.edu.tr

Ayse Cicek

Always discuss trial participation with your own doctor first.

Locations (1)

Istanbul Medipol University HospitalIstanbul, Bagcilar, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07436806