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EXORA Block vs Epidural Analgesia in Gynecological Surgery

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Study completion pushed from Oct 1, 2026 to Nov 1, 2026
    • Eligibility criteria expanded, about 8 words
    • Secondary endpoints: details revised at 2 of 5 entries
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 prospective observational study aims to compare the effects of the EXORA block and epidural analgesia on postoperative pain control and quality of recovery in patients undergoing gynecological surgery. Quality of recovery will be assessed using the Quality of Recovery-15 (QoR-15) questionnaire, and postoperative pain will be evaluated using the Visual Analog Scale (VAS).
Trial Details
NCT Number NCT07346872
Lead Sponsor Bursa Yuksek Ihtisas Training and Research Hospital
Conditions
(from sponsor)		 Pain, Postoperative Pain
Related terms Pain, Postoperative Pain
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov