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
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