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临床试验/NCT01705808
NCT01705808终止3 期

Administration of Protein C Concentrates in Adult Critically Ill Septic Patients

Università Vita-Salute San Raffaele1 个研究点 分布在 1 个国家开始时间: 2012年9月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
终止
试验地点
1
主要终点
Composite endpoint of number of participant with mortality and/or prolonged ICU stay

研究概览

简要总结

Severe sepsis and septic shock are life threatening medical emergencies and are among the most significant challenges in critical care. Case reports and case series suggest that plasma-derived protein C concentrate may improve the outcome of patients with acquired protein C deficiency. Evidence has accumulated on the clinical relevance of the PC pathway in modulating overwhelming inflammation and preventing coagulation derangements, two key mediators of organ damage, and thus of mortality and morbidity, in sepsis. The experience collected through these studies shows that PC is safe, in that it is not associated with bleeding or severe allergic complications,and possibly useful, at least to improve the coagulation abnormalities brought about by sepsis. Unfortunately, however, all we know comes from case series or case reports or an underpowered randomized controlled study. A randomized clinical trial, adequately powered for mortality or clinically relevant outcome, is necessary to confirm PC efficacy.The aim of this study is to demonstrate that Protein C zymogen has clinically relevant implications in terms of reduction of thromboembolic events, 30 days mortality, length of intensive care and hospital stay, time on mechanical ventilation, length of ICU and hospital stay. The study will also confirm that there is no bleeding concern with the use of Protein C concentrates.The study drug will be administered in the Intensive Care Unit for 72 hours and the patients observed till ICU discharge. Telephone followup will be performed at 30 days and at one year.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Written informed consent
  • Age > 18 years
  • At least one of the following 3 criteria:
  • venous-venous extra corporeal membrane oxygenation (ECMO) for septic adult respiratory distress syndrome (ARDS)
  • septic disseminated intravascular coagulopathy (DIC)
  • sepsis induced organ dysfunction associated with a clinical assessment of high risk of death

排除标准

  • Previous unusual response to PC or any of their components (murine proteins and heparin)
  • PC administration or inclusion in other randomized protocols in the previous 30 days
  • Do not resuscitate orders
  • Refractory cardiogenic shock

研究组 & 干预措施

Protein C concentrate

Experimental

干预措施: Protein C concentrate (Drug)

Placebo

Placebo Comparator

干预措施: Protein C concentrate (Drug)

结局指标

主要结局

Composite endpoint of number of participant with mortality and/or prolonged ICU stay

次要结局

未报告次要终点

研究者

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

Giovanni Landoni

Head of Research, Department of Anesthesiology and Intensive Care

Università Vita-Salute San Raffaele

研究点 (1)

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