NCT03807648已完成不适用
Intermountain Utah Study Evaluating the Implementation of Lactated Ringers as Standard Resuscitation Fluid Starting in Emergency Department
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 200,000
- 试验地点
- 1
- 主要终点
- Number of participants with major Adverse Kidney Events
研究概览
简要总结
To study the difference in mortality and major adverse kidney events during and after treatment in the emergency department with intravenous fluids per standard of care at 30 days before and after the system-wide implementation.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adult patients (≥18 years) receiving a minimum of 1000ml of intravenous fluids starting in the emergency department per standard of care
排除标准
- •Patients aged ≤17 years
- •Previously enrolled patients with >1 ED admission within the 30-day follow-up period
结局指标
主要结局
Number of participants with major Adverse Kidney Events
时间窗: within 30 days or at hospital discharge
death from any cause, new renal replacement therapy or persistent renal dysfunction
LR IV Fluids administered
时间窗: Through study completion (an average of 1 year)
Proportion of LR IV fluids following implementation
次要结局
- Rate of hospital admission and readmission(Within 30 days of initial ED encounter)
- Cost(Through study completion (an average of 1 year))
研究者
研究点 (1)
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