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临床试验/NCT00750997
NCT00750997终止不适用

Hypertonic Modulation of Inflammation Following Injury

University of Washington2 个研究点 分布在 2 个国家目标入组 119 人开始时间: 2007年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
119
试验地点
2
主要终点
neutrophil activation

研究概览

简要总结

This project seeks to determine the effect of prehospital resuscitation with hypertonic saline vs. conventional crystalloids on the inflammatory response after injury. The leading cause of late mortality following injury is multiple organ dysfunction syndrome (MODS), which results from a dysfunctional inflammatory response after injury. Previous studies suggest that hypertonic saline may be beneficial by modulating this initial response and decreasing subsequent organ injury. This project takes advantage of a unique opportunity, afforded by an NIH-funded multi-center clinical trial of hypertonic resuscitation (conducted by the Resuscitation Outcomes Consortium), to obtain blood samples from patients enrolled in this trial to analyze inflammatory responses early after hypertonic vs. conventional resuscitation. This study was an ancillary study to the main randomized clinical trial and thus prospective observational in nature

The proposed study will be carried out in experiments grouped in three Specific Aims: Aim 1 provides a thorough investigation of the immunomodulatory response following hypertonic resuscitation with regard to neutrophil, monocyte, and T cell responses at serial time points after injury and resuscitation. Aim 2 comprises experiments to investigate the mechanisms by which hypertonicity may alter inflammatory cell signaling. Aim 3 seeks to correlate the laboratory findings with clinical endpoints reflective of immune dysfunction including inflammation, organ failure, nosocomial infection, and sepsis.

The investigators hypothesize that hypertonic resuscitation will be associated with modulation of the excessive inflammatory response seen after injury and thus will result in reduced rates of inflammatory organ injury.

详细描述

This was an ancillary study to the larger clinical trials of prehospital hypertonic resuscitation conducted by the resuscitation outcomes consortium. This study investigated markers of immune function and coagulation in a subset of patients enrolled in the larger trials at two of the clinical sites. Four publications detail the results please see references

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
15 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Blunt or Penetrating trauma with prehospital systolic blood pressure < 70 or 70-90 mmHg with Heart rate > 108 OR Blunt trauma with prehospital Glasgow coma score <= 8

排除标准

  • Age < 15 yrs
  • Known prisoners
  • Pregnancy
  • Ongoing Cardiopulmonary resuscitation (CPR)
  • Burns < 20%
  • Hypothermia < 28 C
  • > 2 liters intravenous fluid prior to study fluid administration
  • > 4 hour from time of dispatch

研究组 & 干预措施

Hypertonic saline

Hypertonic resuscitation

干预措施: hypertonic saline (Drug)

结局指标

主要结局

neutrophil activation

时间窗: Emergency department admission

several parameters of neutrophil activation were assessed

次要结局

  • Endothelial cell activation(Emergency department admission)
  • monocyte activation(Emergency department admission)
  • coagulation parameters(Emergency department admission)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eileen Bulger

Professor, Surgery

University of Washington

研究点 (2)

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