JPRN-UMIN000010704已完成未知
Comparing study of the efficiency and safety in actual use of two kinds of long-acting ESA for renal anemia in hemodialysis patients - Evaluation analysis for the treatment of renal anemia : two new long-acting ESAs randomised comerison trial:EARNEST STUDY
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Women who are pregnant, breastfeeding, or possibly pregnant Patients who have myocardial infarction,pulmonary embolism or stroke Hypersensitivity to epoetin beta pegol or darbepoetin alfa Patients who have malignant tumor (including hematologic malignancy), severe infection, Hemolytic anemia, hemolytic anemia, or apparent hemorrhagic lesion Patients whose AST or ALT level was 100 IU/L or higher in the latest examination before enrollment Patients who are judged ineligible by the investigator/sub-investigator
研究者
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