跳至主要内容
临床试验/EUCTR2014-003680-38-NL
EUCTR2014-003680-38-NL进行中(未招募)不适用

Pharmacokinetics of two different high dose regimes of intravenous vitamin C in critically ill patients - Pharmacokinetics of two different high dose regimes of intravenous vitamin C in critically ill patie

VU university medical center0 个研究点开始时间: 2015年3月4日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Sepsis or SIRS (systemic inflammatory response syndrome), after major surgery or trauma
  • Non-neurological sequential organ failure score >6
  • Expected length of ICU stay > 96 hours
  • Informed consent by patient or legal representative
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 10
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • Admission after out of hospital cardiac arrest
  • Prior use of supplemental vitamin C in the week before
  • Major bleeding
  • Pre-existent renal insufficiency defined as an eGFR of < 30 ml/min/1.73 m2 (stadium 4-5)
  • Expected need for renal replacement therapy within 48 hours
  • Known glucose 6-phosphate dehydrogenase deficiency
  • History of urolithiasis or oxalate nephropathy
  • Previous use of prolonged high dose vitamin C supplements
  • Hemochromatosis

研究者

发起方
VU university medical center

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