Effect of Different Concentrations of Sevoflurane for Anesthesia Induction in Pediatric Ophthalmic Surgery

This randomized controlled trial aims to compare the effectiveness and safety of 6% versus 8% sevoflurane inhalation induction in pediatric patients undergoing minor ophthalmic surgery. The primary outcome is emergence agitation assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale. Secondary outcomes include hemodynamic parameters, induction time, recovery time, and adverse events.

NCT Number	NCT07450495
Lead Sponsor	Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Conditions	Chalazion
Enrollment	80 participants
Start Date	2025-02-25
Primary Completion	2026-02-25 (estimated)
Study Completion	2026-04-01 (estimated)
Updated on ClinicalTrials.gov	2026-03-04