ChiCTR1800016517已完成Unknown
Comparison of total intravenous anesthesia versus a propofol target controlled infusion combined with low MAC sevoflurane
天津医科大学总医院1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2016年10月17日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- 安全性
研究概览
简要总结
To compare total intravenous anesthesia (TIVA) to 2 groups of combined propofol and sevoflurane anesthesia under 1 MAC anesthesia to determine which technique could provide more favourable overall outcomes in terms of CVS stability, recovery time, consumption of intravenous anesthetics and postoperative side effects.
研究设计
- 研究类型
- Interventional
- 主要目的
- 随机平行对照
- 盲法
- None
入排标准
- 年龄范围
- 20 至 65（—）
- 性别
- All
入选标准
- •Aged 20-65 years, with American Society of Anesthesiologists (ASA) I-II physical status, BMI < 30 kg/m2 and due for elective abdominal, gynecological and lower limb surgeries under general anesthesia
排除标准
- •Uncontrolled hypertension, diabetes, endocrinal disorders, neurological; Disorders including epilepsy, hepatic and renal impairment, neuromuscular disorders, BMI >30kg/m2, History of allergy, pregnant patients, patients on drugs which interfere with neuromuscular relaxants as anticonvulsants and aminoglycosides.
研究组 & 干预措施
P
Control
PS1
propofol + sevoflurane 1%
PS2
propofol + sevoflurane 1.5%
结局指标
主要结局
安全性
时间窗: Before induction of anesthesia until the recovery period
次要结局
未报告次要终点
研究者
研究点 (1)
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