IRCT201102195864N1已完成2 期
The Effect of Intravenous and Oral Iron Administration on Responsiveness to Synthetic Erythropoietin in Hemoglobin Increase of Hemodialysis Patients
Vice chancellor for research, Golestan Medical Sciences University0 个研究点目标入组 42 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 42
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
- no limit 至 no limit（—）
- 性别
- All
入选标准
- •Receiving hemodialysis therapy for at least 6 months; having dossier in hemodialysis ceneter; three time hemodialysis weekly and four hours for each session; hemoglobin less than 10 g/dl; history of seven weeks treatment with subcutaneous erythropoietin (2000 units, three times weekly at the end of each dialysis sessions).
- •Exclusion criteria:
- •Bone marrow malignancy; evidence of chronic infection; evidence of significant bleeding (decrease in Hb level > 2g/dL during the past 3 months); hemoglobinopathies; myelodysplastic syndrome.
排除标准
- 未提供
研究者
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