临床试验/NCT02738164

NCT02738164已完成不适用

Validation of the SEPSIS-3 Criterion for Sepsis and Septic Shock in the Emergency Department

Societe Française de Medecine d'urgence27 个研究点分布在 4 个国家目标入组 879 人开始时间: 2016年5月最近更新: 2016年7月19日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方
入组人数: 879
试验地点: 27
主要终点: In hospital mortality

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Investigators aim to evaluate the SEPSIS 3 criterion for "sepsis" and "septic shock" in a prospective manner.

Investigators will evaluate qSOFA performances and other SEPSIS 3 criterion in a population of emergency patients with infection

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: 否

入选标准

•Adult that present to the emergency department
•Diagnosis of infection by the treating emergency physician

排除标准

•Refuse to participate
•pregnancy
•Low acuity infection (localised, not requiring general treatment, without any abnormal vital parameters)

结局指标

主要结局

In hospital mortality

时间窗: 30 days

次要结局

Length of hospital stay(30 days)
admission in ICU(30 days)
length of ICU stay more than 72 hours(30 days)

研究者

发起方

Societe Française de Medecine d'urgence

申办方类型

Other

责任方

Sponsor

研究点 (27)

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