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临床试验/NCT01354197
NCT01354197已完成不适用

Multicenter Study of Outcome and Adverse Events in Surgical Intensive Care Unit of Thai University Hospital

Royal College of Anesthesiologists of Thailand9 个研究点 分布在 1 个国家目标入组 4,652 人开始时间: 2011年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
4,652
试验地点
9
主要终点
Overall Mortality

研究概览

简要总结

The study observed the 28 days mortality of 9 participated University base surgical intensive care unit (SICU) as well as the occurrence of adverse events in SICU.

详细描述

The adverse events included pulmonary aspiration, pulmonary emboli, drug error, new stroke, symptomatic deep vein thrombosis, pneumothorax, unplanned extubation, upper GI hemorrhage, myocardial infarction, abdominal hypertension, acute lung injury(ALI)/acute respiratory distress syndrome (ARDS), re-intubation within 72 hours, delirium, cardiac arrest, new arrhythmia, acute kidney injury, sepsis

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • All SICU admission patients

排除标准

  • Age < 18 years

结局指标

主要结局

Overall Mortality

时间窗: 28 days

Number of Participants who Did Not Survive up to 28 days after surgical ICU admission

次要结局

  • Readmission to ICU(3 days)

研究者

发起方
Royal College of Anesthesiologists of Thailand
申办方类型
Other
责任方
Sponsor

研究点 (9)

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