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PRevention of End stage kidney disease by Darbepoetin Alfa In CKD patients with non-diabeTic kidney disease. - PREDICT

PREDICT steering committee0 个研究点目标入组 440 人开始时间: 2011年10月27日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
440

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 85years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Diabetes (HbA1c 6.4% IFCC) 2) CKD patients treated with ESA other than epoetins. 3) CKD patients treated with epoetin 36000 IU or more. 4) Hypertension (180/10mmHg and higher) 5) Heart failure (NYHA III and IV) 6) malignancy, hematological disorder 7) malnuturition 8) Active and continuous gastrointestinal tract bleeding 9) ANCA associated glomerulonephritis, acute infection, active SLE 10) CKD patients who will be started dialysis or will receive tranplantation 11) Myocardial infarction within last 6 months 12) Stroke or plumonary embolism within last 12 months 13) Severe allergy 14) Pregnant woman or CKD patients who wish to be pregnant 15) Allergy against erythropoetin 16) CKD patients who is not appropriate to entry the clincal trial

研究者

发起方
PREDICT steering committee

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