跳至主要内容
临床试验/NCT01967602
NCT01967602Unknown不适用

Biomarker of Lung Injury in ARDS Patients Receiving ECMO Support

National Taiwan University Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2011年10月最近更新:
适应症

试验速览

阶段
不适用
入组人数
70
试验地点
1
主要终点
Mortality or multi-organ failure

研究概览

简要总结

The goal of this project is to find a marker expression that the investigators can use to trace symptom progression and develop a more efficient therapy to enhance ARDS patient survival rate and better post-ICU life quality.

详细描述

The investigators will first identify acute respiratory distress syndrome (ARDS) patients receiving ECMO support in ICU at National Taiwan University Hospital, and then collect blood, urine and bronchioalveolar lavage fluid (BALF) samples at different time points: before setting up ECMO, 2, 6, 12, 24, 72 hours,5 and 14 days after ECMO installment, time to wean ECMO and the day removing ECMO and leaving ICU. From the samples, the free radicals, cytokines (IL-1, IL-6, IL-8, IL-18,tumor necrosis factor-α, transforming growth factor-β), and inflammasome- related markers, immune cell responses and other biochemical markers would be measured. The novel biomarkers to predict the outcome of the patient will be identified.

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

  • >18 years old
  • ARDS, needing ECMO support

排除标准

  • pre-existing sepsis
  • pre-existing chronic renal failure (dialysis dependent), liver failure other diseases precluding chance of survival.

结局指标

主要结局

Mortality or multi-organ failure

时间窗: 7 days

Patients who survived for more than 7 days after ECMO treatment were defined as survival, and non-survival patients were defined as expired or multiple organ failure incompatible with life within 7 days after ECMO installation.

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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