NL-OMON55764已完成不适用
Insufficient oxygenation in septic patients: the INOX Sepsis Study - the INOX Sepsis Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 72
研究概览
简要总结
Trial ended prematurely
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Age of patient is at least 18 years
- •- Patients diagnosed with sepsis in the emergency department or hospital ward,
- •including patients with possible COVID-19
- •- Patients are admitted to the ICU via the hospital ward or emergency department
- •- Informed or deferred consent is given either by the patient or if the patient
- •is too ill to give informed consent, by his or her legal representative
- •- Patients have an arterial catheter in situ, since blood samples will be taken
- •for the study. Most patients admitted to the ICU have an arterial catheter in
- •place since it is part of standard care.
排除标准
- •-Patients younger than 18 years
- •-Patients with sepsis discharged after emergency department visit
- •-Patients admitted with sepsis to a hospital ward other than the ICU after
- •emergency department visit
- •-Patients without a legal representative will be excluded since no informed
- •consent can be given
- •-Patients known with porphyria and/or photodermatosis will be excluded, due to
- •the risk of phototoxicity
- •-Patients with hypersensitivity to the active substance or to the plaster
- •material of ALA (5-aminolevulinic acid)
- •-Pregnant or breast feeding women since there is no adequate data form the use
- •of ALA in pregnant or breast feeding women
- •-Insufficient comprehensibility of the Dutch language
研究者
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