NCT00983281已完成不适用
Use of Hextend in Trauma
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,714
- 试验地点
- 1
- 主要终点
- Mortality
研究概览
简要总结
This is a chart review of all trauma patients during the specified time period. The purpose of this study is to examine the effects of resuscitation with hextend after trauma, in the adult population. The authors hypothesize that when compared to patients resuscitated with standard of care, resuscitation with Hextend will result in a mortality difference.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Admission to the trauma center
排除标准
- •Pregnant women, children, psychiatric patients and prisoners.
研究组 & 干预措施
Hextend
Patients that received Hextend as part of their fluid resuscitation.
干预措施: Hextend (Drug)
Standard of Care
Patients that received standard fluid resuscitation but no Hextend.
干预措施: Hextend (Drug)
结局指标
主要结局
Mortality
时间窗: Overall inpatient mortality upon discharge from the hospital with a mean length of stay of 8 days.
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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