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临床试验/NCT01690845
NCT01690845Unknown2 期

Molecular Adsorbent Recirculating System (MARS®) for the Treatment of Patients With Hypoxic Hepatitis - a Prospective Randomized Controlled Clinical Study

Medical University of Vienna4 个研究点 分布在 2 个国家目标入组 40 人开始时间: 2012年6月最近更新:
适应症

试验速览

阶段
2 期
入组人数
40
试验地点
4
主要终点
difference of the indocyanine plasma disappearance rate (ICG-PDR)

研究概览

简要总结

Hypoxic hepatitis (HH) is reported to be the most frequent cause of elevated aminotransferase levels in hospital. Up to 10 % of critically ill patients develop HH during the course of their intensive care unit (ICU) stay. Occurrence of HH is a life threatening event and ICU-mortality is reported to be up to 60%. Early therapeutic intervention is of central prognostic importance in patients with HH to improve the hemodynamic impairment as early as possible, to reduce hyperammonemia and hepatic encephalopathy, to avoid progression of organ failure and to improve outcome. Studies reported that Molecular Adsorbent Recirculating System (MARS®) therapy improved the hemodynamic situation in patients with acute and acute on chronic liver failure. The study hypothesis is that MARS® therapy in critically ill patients with severe HH improves hepatic hemodynamics and function and consecutively the course of the disease. 40 patients with suffering of severe HH with aminotransferase levels > 40 times the upper limit of normal of more than 12 hours will be randomized 1:1 to MARS® therapy (n=20) or conventional therapy (n=20). 4 MARS®-sessions will be performed on three consecutive days, each for at least 12 hours. Treatment will be continued under special circumstances. The maximum duration of the treatment phase is 7 days. The primary endpoint is the difference of the indocyanine plasma disappearance rate at day 7. The expected duration of the study is 2 years.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • presence of severe hypoxic hepatitis with aminotransferase levels > 40 times the upper limit of normal
  • duration of hypoxic hepatitis more than 12 hours
  • age >/= 18 years

排除标准

  • age < 18 years
  • pregnancy
  • DNR - order
  • liver cirrhosis
  • Cardiopulmonary resuscitation with unknown neurological outcome and/or hypoxic brain damage
  • Expected survival of less than 24 hours

结局指标

主要结局

difference of the indocyanine plasma disappearance rate (ICG-PDR)

时间窗: Days 1-7

The primary endpoint will be the difference of the indocyanine plasma disappearance rate (ICG-PDR) at day 7. Only in case of major differences in baseline values of ICG-PDR we will use the change from baseline to day 7 of ICG-PDR (delta ICG-PDR) as outcome. Assuming normal distribution of ICG-PDR, we will formally test the null-hypothesis of no difference between intervention group and control using an independent sample t-test. The assumption of a normal distribution will be founded on visually inspecting a histogram and using the Shapiro Wilks test for normal distribution. If the assumption of normality does not hold data will be compared using the Mann-Whitney U-test. A p-level of \< 0.05 will be considered statistically significant. Furthermore a linear random coefficient model will be used to incorporate daily measurements of ICG-PDR during the course of the study in terms of a repeated measures design.

次要结局

  • number of vasopressor free days(28 days)
  • 28 day mortality(28 days)
  • number of organ failure on day 7(7 days)
  • hospital - length of stay(1-90)
  • duration of vasopressor support(1-28)
  • ICU - length of stay(1-28)
  • 7-day mortality(7 days)
  • number of organ failure on day 28(28 days)
  • markers of liver function(1-28)
  • systemic hemodynamics(7 days)
  • number of complications of HH(1-28)
  • biomarkers(0-28)
  • duration of mechanical ventilation(1-28)
  • duration of renal replacement therapy(1-28)
  • necessity of renal replacement therapy(1-28)
  • 90 days mortality(90 days)

研究者

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

Valentin Fuhrmann

Associate Professor

Medical University of Vienna

研究点 (4)

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