EUCTR2007-001089-33-NL进行中(未招募)1 期
Infusion of a single dose of erythropoietin to Prevent Injury in an Ischemia Reperfusion forearm model - A randomised cross-over study to evaluate if infusion of a single dose of EPO protects against ischemia-reperfusion injury in man. - IPIIR
niversity Medical Center Groningen, dept. of Cardiology0 个研究点目标入组 18 人开始时间: 2008年5月29日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 18
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
- •Healthy volunteers between 18 and 40 years of age.
- •Volunteers are not allowed smoking 24 hours before the start of the experiment.
- •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
- •Hypertension (SBP >140 mmHg, DBP >90 mmHg).
- •Diabetes Mellitus (DM) (fasting glc >6.9 mmol/l, glc >11.0 mmol/l).
- •Hypercholesterolemia.
- •Renal dysfunction (eGFR < 60 ml/min, calculated using MDRD formula).
- •Any known hypersensitivity/allergic reaction to one of the constituents of Epoetin Alfa.
- •A history of use of any form of EPO.
- •Any current medication use.
- •Cardiovascular disease in medical history.
- •Smoking less than 24 hours prior to Epoetin alpha infusion.
- •Participation in research in the last 5 years in which any form of radioactivity was used.
- •No participation in any research trial in the last 30 days or 5 times the half-life of the used substance.
研究者
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