本隨機對照試驗旨在比較 6% 對比 8% sevoflurane 吸入誘導於接受小型眼科手術的小兒患者中的有效性與安全性。主要結局為使用小兒麻醉甦醒期譫妄（PAED）量表評估的甦醒期躁動。次要結局包括血流動力學參數、誘導時間、恢復時間及不良事件。
適應症：Chalazion
收案條件
納入條件
- Children aged 1 to 6 years (12-72 months)
- Scheduled to undergo minor ophthalmic surgery (e.g., chalazion excision) under general anesthesia
- American Society of Anesthesiologists (ASA) physical status I
- Assessed as suitable for inhalation anesthesia by anesthesiologists
- Written informed consent obtained from parents or legal guardians
排除條件
- ASA physical status II or higher
- Known hepatic or renal dysfunction
- Congenital heart disease
- History of malignant hyperthermia
- Known allergy to sevoflurane
- History of asthma or severe respiratory disease
- Upper respiratory tract infection within the past 4 weeks
- Anticipated difficult airway
- Refusal of participation by parents or legal guardians
收案條件維持 ClinicalTrials.gov 原始英文登錄資料，實際收案資格以研究團隊的正式評估與受試者同意書為準。資料來源：ClinicalTrials.gov，每兩週自動更新，最後同步：2026年10月8日。