跳至主要内容
临床试验/NL-OMON38854
NL-OMON38854已完成不适用

Pharmacokinetics of nAdroparin in venous thromboembolism Prophylaxis in critically ill pAtients - an observational pilot study - The PAPA study

Meander Medisch Centrum0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • * The patient is at least 18 years of age.
  • * The patient is admitted to the intensive care unit.
  • * The patient is already treated with nadroparin for VTE prophylaxis, or, is eligible for treatment with nadroparin for such reasons.
  • * The patient already has a catheter to obtain the necessary blood samples.

排除标准

  • * Acute and life-threatening complications that require immediate patient treatment, as decided by the intensive care physician.
  • * The patient is admitted to the ICU for routine post-operative intensive care monitoring
  • * The patient is treated with a therapeutic dose of nadroparin

研究者

发起方
Meander Medisch Centrum

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