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Low Versus Standard Volume EXORA Block in Laparoscopic Cholecystectomy

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 2 months later Nov 1, 2026 → Jan 1, 2027
See other at-risk trials from Fayoum University Hospital

Record History

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  1. Recruitment openedv4 Show 4 more changesShow less
    • Primary completion pushed from Nov 1, 2026 to Jan 1, 2027
    • Study completion pushed from Nov 2, 2026 to Jan 2, 2027
    • Start date changed from estimate of Apr 10, 2026 to Apr 12, 2026
    • Site details revised
  2. Secondary endpoints revised (13)v3
  3. Secondary endpoints: 10 to 13v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The original EXORA block used high local anesthetic volume (50 mL total), raising concerns about local anesthetic systemic toxicity (LAST). In such a bilaterally administered regional technique, evaluating the efficacy of a reduced-volume approach is warranted to maximize patient safety.
Trial Details
NCT Number NCT07507799
Lead Sponsor Fayoum University Hospital
Conditions
(from sponsor)		 Pain, Postoperative, Post Operative Analgesia
Related terms Postoperative Pain
Enrollment 96 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov