Clinical Trial

Minimal- Versus High-Flow Sevoflurane and Emergence Agitation in Pediatric Surgery

Active, Not Recruiting
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Summary
This study aims to evaluate the effects of minimal-flow sevoflurane compared with high-flow sevoflurane during maintenance of general anesthesia on postoperative emergence agitation in opioid-free pediatric infraumbilical surgeries. Patients will be randomly assigned to receive either opioid-free minimal-flow anesthesia combined with caudal block or opioid-free high-flow anesthesia combined with caudal block. The primary outcome is emergence agitation assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale and the Watcha scale. Secondary outcomes include the incidence of postoperative nausea and vomiting and recovery characteristics. In addition, all patients will be followed up via telephone at 3 months postoperatively to assess the presence of persistent chronic or neuropathic pain at the surgical site. The findings of this study may contribute to optimizing anesthesia strategies and improving postoperative outcomes in pediatric patients.
Trial Details
NCT Number NCT07635004
Lead Sponsor Ankara City Hospital Bilkent
Conditions Postoperative Agitation, Emergence Agitation
Enrollment 80 participants
Start Date 2026-04-22
Primary Completion 2026-06-22 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-09