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临床试验/NCT00825357
NCT00825357已完成不适用

Biological Markers to Identify Early Sepsis and Acute Lung Injury

Chimei Medical Center1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2006年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
The present study will focus on testing 'biological markers' to identify patients with sepsis and acute lung injury in early stage.

研究概览

简要总结

There are no clear markers to identify sepsis and acute lung injury at early stage in clinical settings which would result in improved survival of the patients. In collaboration with the research team led by Dr. Zhang at St. Michael's Hospital, Toronto, we have initiated a pilot study looking for biological markers to detect severe sepsis and ARDS. We have found that human neutrophils peptides (a-defensins), certain coagulation variables and cytokine levels are very sensitive markers to differentiate severe sepsis, ARDS from cardiovascular diseases in ICU patients. These findings may provide valuable information for therapeutic guideline in clinical practice. The present study will focus on testing 'biological markers' to identify patients with sepsis and acute lung injury. We will examine the roles of three components of markers including inflammation, neutrophil activation and coagulation. We are hoping that this proposed translational research will help develop novel therapeutic strategy in sepsis and acute lung injury patients.

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

入选标准

  • Meet diagnostic criteria of ≧2 SIRS or acute lung injury.
  • Get agreement of patient's attending physician and inform consent form patient or family.

排除标准

  • Use Antibiotics over 24 hrs(only SIRS group).
  • Active bleeding.
  • Pregnancy.
  • Active Cancer (refer to malignancy which is recently diagnosed, under treatment, or relapsed)
  • VS or Subject or Family refuse

结局指标

主要结局

The present study will focus on testing 'biological markers' to identify patients with sepsis and acute lung injury in early stage.

时间窗: 72 hrs

次要结局

未报告次要终点

研究者

发起方
Chimei Medical Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kuo-Chen Cheng

Chief

Chimei Medical Center

研究点 (1)

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