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SPSIP vs ESP Block for Analgesia After Rib Fracture Surgery

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Study description expanded, about 6 wordsv3
  2. Enrollment increased: 50 → 60 participants
    • Study description shortened, about 9 words
    • Site contact updated
    • Study title shortened, about 7 words
    v2
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 randomized clinical trial aims to evaluate and compare the analgesic efficacy of the Serratus Posterior Superior Intercostal Plane (SPSIP) block and the Erector Spinae Plane (ESP) block in patients undergoing surgical stabilization of rib fractures. The primary outcome is the Visual Analog Scale (VAS) score within the first 24 hours after surgery. Secondary outcomes include total opioid consumption, requirement for rescue analgesia, block performance time, block-related and systemic side effects (hematoma, pneumothorax, local anesthetic systemic toxicity, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, and quality of recovery assessed using the QoR-15 questionnaire.
Trial Details
NCT Number NCT07553208
Lead Sponsor Antalya City Hospital
Conditions
(from sponsor)		 Rib Fracture, Postoperative Pain, Thoracic Trauma
Related terms Postoperative Pain, Rib Fractures
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov