TCTR20170808001进行中（未招募）4 期
A Retrospective Study of the Efficacy and Safety of Hema-Plus (Recombinant Human Erythropoietin Alfa) in Patients with Chronic Kidney Disease who continuously used Hema-Plus at Siriraj Hospital
Apexcela Co., Ltd.0 个研究点目标入组 200 人开始时间: 2017年8月8日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 0 N/A (No limit) 至 0 N/A (No limit)（—）
- 性别
- All
入选标准
- •Each patient included in the review must meet all of the following criteria to be in this study:
- •1.Presented with chronic kidney disease
- •2.History of receiving Hema-Plus for at least 6 months during the study period
排除标准
- •1.Subjects who met inclusion criteria but their medical records are not available for access.
研究者
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