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临床试验/NCT01681758
NCT01681758已完成2 期

A Before-and-after Assessment of Pulse Pressure Variation Guided Fluid Therapy in Cardiac Surgery Patients Receiving Mandatory Mechanical Ventilation

Austin Health2 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2012年1月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
Austin Health
入组人数
104
试验地点
2
主要终点
Mean amount of fluid given in the first 24 hours after surgery

研究概览

简要总结

We aim to test the hypothesis that fluid therapy based on pulse pressure variation (PPV) in patients after cardiac surgery who are mechanically ventilated leads to a significant decrease in the amount of fluid given to such patients in the first 24 hours after surgery

详细描述

  1. The investigators will study patients after cardiac surgery
  2. The investigators will collect data on standard care in pre-intervention population
  3. The investigators will collect demographic and clinical data
  4. The investigators will collect biochemical data in the first 24 hours after surgery
  5. The investigators will collect biochemical, physiological and clinical outcome data
  6. The investigators will compare the standard care and intervention period data

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • immediately after ICU admission after cardiac surgery
  • mandatory mechanical ventilation -

排除标准

  • Pressure support ventilation
  • Intra-aortic balloon counterpulsation

结局指标

主要结局

Mean amount of fluid given in the first 24 hours after surgery

时间窗: 24 hours

all intravenous fluid administered

次要结局

  • Physiological outcome(24 hours)

研究者

发起方
Austin Health
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Rinaldo Bellomo

Director of ICU Research

Austin Health

研究点 (2)

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