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临床试验/NCT03190408
NCT03190408已完成不适用

Observation of Variation in Fluids Administered and Characterization of Vasopressor Requirements in Shock

Montefiore Medical Center1 个研究点 分布在 1 个国家目标入组 1,639 人开始时间: 2017年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,639
试验地点
1
主要终点
Method used to guide volume resuscitation

研究概览

简要总结

To conduct a multicenter observational cohort study to determine the variability in fluid resuscitation in shock in a broad range of areas in hospitals and treatment areas.

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

入选标准

  • Age ≥ 18 years admitted to the participating hospital.
  • Patients in the emergency department, intensive care unit, PACU, or any hospital floor. For patients not in the ICU, there must be plans to transfer to an intensive care unit when an ICU bed is available for patient.
  • Patients with shock as defined by:
  • Need for vasopressor (dopamine, norepinephrine, or epinephrine at any dose) to keep MAP > 65 mmHg Or
  • Systolic BP < 90 mmHg

排除标准

  • Patients previously enrolled into this study.
  • Patients who were in the operating room at time of shock and fluid bolus.
  • Patients admitted to an ICU after cardiac surgery Patients with primarily cardiogenic shock as etiology for their shock
  • Patients transferred from another hospital or emergency room to the study hospital.

结局指标

主要结局

Method used to guide volume resuscitation

时间窗: 7 days

Characterize the method used to guide volume resuscitation and vasopressor use in patients with shock

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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Variation in Fluids Administered in Shock | 临床试验