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临床试验/NCT04901338
NCT04901338已完成不适用

Cytokine Hemoadsorption in ECMO Patients

University Medical Centre Ljubljana1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2017年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
25
试验地点
1
主要终点
Haemodynamic stabilization

研究概览

简要总结

Cytokine hemoadsorption is a novel therapy used to improve outcome in critically ill patients with a dysregulated cytokine response and hemodynamic instability. Patients on extracorporeal membraneous oxygenation (ECMO) often develop severe systemic inflammatory response syndrome (SIRS). Cytokine removal using different types of hemoadsorption devices is believed to block the vicious circle of inflammation dysregulation when other basic therapeutic measures fail. To date there are very limited reports on ECMO and cytokine hemoadsorption combination therapy. The aim of this retrospective study is to evaluate feasibility and effectiveness of hemoadsorption in veno-arterial and veno-venous ECMO patients.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

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

  • VA/VV ECMO
  • hemoadsorption
  • Age ≥ 18 years

排除标准

  • no additional exclusion criteria after being eligible for ECMO

结局指标

主要结局

Haemodynamic stabilization

时间窗: Within 12 hours after hemoadsorption

Decreased need for vasopressors according to vasoactive-inotropic score and increase in mean arterial pressure

次要结局

  • Lactate, interleukin-6, C-reactive protein and procalcitonin clearance(Within 12 hours after hemoadsorption)
  • ICU length of stay(from day of ICU-admission for every 24 hours until date of discharge or death, whichever came first, assessed up to 90 days)
  • Weaning from ECMO(from day of ECMO-implant for every 24 hours until date of weaning or death, whichever came first, assessed up to 90 days)
  • Hospital mortality(from day of hospital admission until date of discharge or death, whichever came first, assessed up to 90 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jernej Berden

Jernej Berden, MD, PhD

University Medical Centre Ljubljana

研究点 (1)

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