To study the incidence of adverse events during intrahospital transport of critically ill patients A prospective observational study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- To analyse adverse events during intrahospital transport of critically illl patients and study patient outcome (survival or death ) within 24 hr .
研究概览
简要总结
This protocol has been prepared as per STROBE (Strengthening the Reporting of Observational studies in Epidemiology) guidelines. After approval from the ethics committee, IGMC Shimla and obtaining the CTRI number, the patients will be recruited in the study following informed written consent by the patients themselves or from the next of their kin . The study cohort will include all critically ill patients of all age group . All qualitative variables will be noted before transport, during transport and after receiving patient in ICU . All qualitative variables Will be tabulated and analysed as frequency and percentage.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 0.00 Day(s) 至 99.00 Year(s)（—）
- 性别
- All
入选标准
- •All critically ill patients of every age who underwent intrahospital transport are included in the study 2)All critically ill patients of either gender who underwent intrahospital transport are included in the study.
排除标准
- •Refusal to participate in study 2)patients who are not critically ill.
结局指标
主要结局
To analyse adverse events during intrahospital transport of critically illl patients and study patient outcome (survival or death ) within 24 hr .
时间窗: 1) before transport for 15 min | 2 During transport | 3) after returning to ICU for 15 min
次要结局
- 1)To determine the nature of problems encountered during intrahospital transport.(2) Preventive strategies which could be put in place to reduce observed adverse events.)
研究者
Shagun Guleria
Indira Gandhi Medical College shimla