临床试验/NCT01021228

NCT01021228已完成不适用

Preconditioning is Indeed Protective

University of Zurich1 个研究点分布在 1 个国家目标入组 257 人开始时间: 2008年8月最近更新: 2009年11月26日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方: University of Zurich
入组人数: 257
试验地点: 1
主要终点: peak ALT and AST levels representing the ischemia-reperfusion injury

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to compare the impact and outcome of continuous volatile anesthesia to continuous intravenous anesthesia and to preconditioning volatile anesthesia in liver surgery.

详细描述

Comparing the impact and outcome of continuous volatile anesthesia to continuous intravenous anesthesia and to preconditioning volatile anesthesia in liver surgery.

研究设计

研究类型: Observational
观察模型: Cohort
时间视角: Retrospective

入排标准

年龄范围: 18 Years 至 90 Years（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•> 18 years
•benign and malign disease
•any type of liver surgery
•inflow occlusion during the liver surgery

排除标准

•< 18 years
•participation on other interventional and treatment randomized controlled trials,
•trauma of the liver
•liver cirrhosis

结局指标

主要结局

peak ALT and AST levels representing the ischemia-reperfusion injury

时间窗: post-operative

次要结局

length of hospital stay, length of ICU stay, blood loss and morbidity (post-operative complications)(post-operative)

研究者

发起方

University of Zurich

申办方类型

Other

研究点 (1)

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