NL-OMON51879尚未招募不适用
Detection of sepsis at the intensive care unit with non-invasive transcutaneous blood gas monitoring. - COSMOS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Sepsis group:
- •Sepsis classified as 2 SIRS criteria and suspected infection
- •Signs of hypoperfusion, requiring noradrenaline administration of at least
- •0.5 µg/min/kg
- •Written informed consent.
- •Control group:
- •No fulfillment of 2 SIRS criteria, nor suspected infection
- •No signs of hypoperfusion, noradrenaline administration of less than or equal
- •to 0.5 µg/min/kg
- •Written informed consent.
排除标准
- •Sepsis group:
- •No sepsis
- •Skin condition contraindicating transcutaneous blood gas measurements.
- •Absence of written informed consent.
- •Control group:
- •Sepsis classified as 2 SIRS criteria and suspected infection
- •Skin condition contraindicating transcutaneous blood gas measurements.
- •Absence of written informed consent.
研究者
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