NCT00527098已完成不适用
Optimal Fluid Resuscitation for Trauma Patients
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 119
- 试验地点
- 1
- 主要终点
- Mortality
研究概览
简要总结
The purpose of this study is to determine if the overall fluid requirements for the first 24 hours after admission will be reduced with Hextend versus a standard of care crystalloid resuscitation fluid.
详细描述
Following severe multi-system traumatic injury, the first 24 hours of standard resuscitation fluid will be either Hextend or crystalloid depending upon attending preference. No tests or interventions will be performed for research purposes.
Data will be collected prospectively from patient medical records and attending clinicians to monitor fluid requirements, hemodynamics and outcome.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Greater than or equal to 18 years old and less than 65 years old
- •Admission with multi-system traumatic injury
- •Admission to the intensive care unit
排除标准
- •Less than 18 or greater than 65 years old
- •Pregnant or lactating
- •No fluid resuscitation
结局指标
主要结局
Mortality
时间窗: From hospital arrival up to an average of 3.5 weeks
次要结局
未报告次要终点
研究者
Kenneth Proctor
Professor
University of Miami
研究点 (1)
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