NCT00613392终止3 期
Antioxidant Supplementation in Trauma Patients
适应症
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 18
- 主要终点
- measures of malondialdehyde level/total antioxidant status and F2 isoprostane
研究概览
简要总结
Administration of antioxidants to trauma patients will improve measures of oxidant stress in the blood
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adult non pregnant non lactating trauma patient
排除标准
- •Renal dysfunction (cre > 2.5 mg/dl)
- •Hepatic dysfunction ( TBili > 3.0 mg/dl)
- •Expected survival < 48 hours
- •Burns over > 20% body surface area
- •Immune-deficiency syndromes
- •Steroid use
结局指标
主要结局
measures of malondialdehyde level/total antioxidant status and F2 isoprostane
时间窗: 7 days
次要结局
未报告次要终点
研究者
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