EUCTR2005-000744-82-AT进行中（未招募）不适用
Impact of rhCu/Zn SOD on inflammation-induced impairment of vascular reactivity - LPS-rhSOD
Medical University Vienna, Dept. of Clinical Pharmacology0 个研究点目标入组 43 人开始时间: 2005年5月23日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 43
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
- Male
入选标准
- •-Men aged between 18 and 45 years
- •-Nonsmoker
- •-Body mass index between 15th and 85th percentile (Must et al. 1991)
- •-Normal findings in medical history and physical examination unless the
- •investigator considers an abnormality to be clinically irrelevant
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-Regular use of medication, abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study
- •-Evidence of hypertension, pathologic hyperglycemia, hyperlipidemia
- •-Treatment in the previous 3 weeks with any drug
- •-Symptoms of a clinically relevant illness in the 3 weeks before the first
- •-History or presence of gastrointestinal, liver or kidney disease, or other
- •conditions known to interfere with distribution, metabolism or excretion of
- •study drugs
- •-Blood donation during the previous 3 weeks
- •-History of hypersensitivity to the trial drug or to drugs with a similar
- •chemical structure
研究者
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