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Analgesic Efficacy of SPSIP Block Versus Paravertebral Block Following Thoracotomy

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Trial completed Show 5 more changesShow less
    • Study completion date changed from estimate of Dec 15, 2026 to Aug 31, 2026
    • Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 3 of 4 entries
    • Site details revised
    • Publications: details revised at 6 of 6 entries
  2. Primary completion pushed from Jul 15, 2026 to Aug 15, 2026v4
  3. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v3
  4. Secondary endpoints: details revised at 2 of 4 entriesv2
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Thoracotomy causes severe postoperative pain that may impair respiratory function and increase complications. This study compares the postoperative analgesic effectiveness of the serratus posterior superior intercostal plane (SPSIP) block and the paravertebral block in patients undergoing thoracotomy. The aim is to determine whether the newly described serratus posterior superior intercostal plane block can serve as a safe and effective alternative to established techniques.
Trial Details
NCT Number NCT07275047
Lead Sponsor Bursa City Hospital
Conditions
(from sponsor)		 Post-thoracotomy Pain
Related terms Agnosia
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov