跳至主要内容
临床试验/KCT0012303
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

The Catholic University of Korea, Seoul St. Mary's Hospital0 个研究点目标入组 50 人开始时间: 2026年7月27日最近更新:
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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