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临床试验/NCT03182335
NCT03182335进行中(未招募)不适用

An Assessment of Vasoactive Medication Dose in Mechanically Ventilated Patients Undergoing Daily Sedation Awakening Trial (SAT)

University of Chicago1 个研究点 分布在 1 个国家目标入组 800 人开始时间: 2014年4月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
800
试验地点
1
主要终点
change in vasoactive drug dose

研究概览

简要总结

To assess the impact of daily awakening from sedation on the amount of vasoactive medication required in the ICU. The hypothesis of this proposal is that the amount of vasoactive drug required to maintain an adequate mean arterial blood pressure will be reduced during a daily awakening from sedation.

详细描述

This observational study will compare mean arterial pressure and vasoactive drug dose recorded at two time points:

  1. prior to awakening from sedation
  2. during the awakening from sedation trial The vasoactive infusion will be titrated to a mean arterial pressure as determined by the medical team prior to study enrollment. Each enrolled patient will have measurements taken only on the first day of enrollment. Enrolled subjects will also have a delirium assessment using the CAM-ICU tool before the awakening from sedation trial and during the awakening from sedation trial.

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

  • •requiring Mechanical ventilation through an endotracheal tube with infusion of sedative or analgesic agent for comfort
  • •requiring vasoactive drug via central venous catheter for the treatment of shock

排除标准

  • •patients receiving Dexmedetomidine as sedative

研究组 & 干预措施

Mechanical Ventilation (MV) with vasoactive infusions

adult ICU patients who are mechanically ventilated with sedative infusion and/or analgesic infusion and also requiring vasoactive drug infusions for the treatment of shock. Patients will be excluded if receiving dexmedetomidine as sedative.

干预措施: sedation awakening trial (Other)

结局指标

主要结局

change in vasoactive drug dose

时间窗: baseline thru study completion on average < 4 hrs

mcg/kg/min baseline dose and nadir dose

次要结局

  • change in mean arterial blood pressure(baseline thru study completion on average <4 hrs)
  • change in prevalence of ICU delirium(baseline thru study completion on average <4hrs)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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