KCT0012303招募中不适用
Establishing Evidence Based Indication of AN69-oXiris and PMX-HP Blood Purification Therapies Based on the Endotoxin Activity Assay in Septic Patients
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 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
- Interventional
- 主要目的
- Treatment
入排标准
- 年龄范围
- 18(Year) 至 No Limit(—)
- 性别
- All
入选标准
- •? Adult patients aged 18 years or older
- •? Patients diagnosed with sepsis or septic shock caused by an intra-abdominal infection, such as peritonitis, according to the Sepsis-3 criteria
- •? Patients who have undergone emergency surgery for source control and in whom surgical source control has been successfully completed
- •? Patients admitted to the Surgical Intensive Care Unit (SICU) for postoperative intensive care
- •? Patients in whom endotoxin activity (EA) can be measured using the Endotoxin Activity Assay (EAA)
- •? Patients determined by an intensivist to require extracorporeal blood purification therapy with either AN69-oXiris or PMX-HP
- •? Patients in whom central venous access can be established and extracorporeal blood purification therapy can be performed
- •? Patients who, or whose legally authorized representatives, have received sufficient information about the study and voluntarily provided written informed consent
排除标准
- •? Pediatric patients under 18 years of age
- •? Patients in whom surgical source control is incomplete or has not been performed
- •? Pregnant or breastfeeding women
- •? Patients who refuse to participate in the study or for whom consent from a legally authorized representative cannot be obtained
- •? Patients concurrently participating in another clinical study
研究者
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