ACTRN12610000693022已完成3 期
A randomised control trial comparing accuracy of two commercially available pharmacokinetic algorithms for total intravenous anaesthesia (TIVA) using Propofol in children aged 1-16 years
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 1 Years 至 16 Years（—）
- 性别
- All
入选标准
- •Children aged 1-16 yrs old having surgery necessitating insertion of an arterial line for intra-operative monitoring
- •American Society of Anesthesiologists (ASA) status 1-3
- •Surgical procedure expected to last between 1-8 hours
排除标准
- •Evidence of severe impairment of respiratory, hepatic, renal or endocrine function
- •Allergy to any constituents of Propofol
- •Patients with known intra or extra-cardiac shunts” (that allow mixing of arterial and venous blood, affecting measurements of Propofol)
- •Patients who are intended to receive Ketamine at doses greater than 0.4 mg/kg/hr (may interfere with BIS readings)
- •Treating anaesthetist excluding the patient if unfamiliar with the use of Propofol TCI for anaesthesia maintenance.
研究者
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