Analgesic Effectiveness of SPSIPB Versus Thoracic Epidural and Systemic Opioid Analgesia After VATS (SPSIPB-VATS)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorKaradeniz Technical University

About this trial

This prospective observational study aims to compare the postoperative analgesic effectiveness of three commonly used pain management strategies in video-assisted thoracoscopic surgery (VATS): Serratus Posterior Superior Intercostal Plane Block (SPSIPB), Thoracic Epidural Analgesia (TEA), and systemic opioid analgesia. The study evaluates postoperative pain scores, opioid consumption, and the need for rescue analgesics within the first 24 hours after surgery. By analyzing analgesic performance and safety profiles of these techniques, the study seeks to provide evidence to guide optimal postoperative pain management for patients undergoing minimally invasive thoracic procedures.

Eligibility criteria

Qualifiers

Adults aged 18-75 years

Scheduled for elective video-assisted thoracoscopic surgery (VATS)

ASA physical status I-III

Ability to understand study procedures and provide written informed consent

Disqualifiers

Known allergy or contraindication to local anesthetics or study medications

Coagulopathy or use of anticoagulants not suitable for regional anesthesia

Local infection or skin lesions at the injection site

Severe pulmonary disease (e.g., severe COPD, uncontrolled asthma)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

120 Participants
are grouped into 3 trial groups

Locations

This trial has no locations

Sponsors and collaborators