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临床试验/JPRN-UMIN000011237
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The Relationship between the dose of Epoetin Beta Pegol for treatment of renal anemia and renal prognosis in CKD Patients - The Relationship between the dose of Epoetin Beta Pegol and renal prognosis in CKD Patients

Toda Central General Hospital0 个研究点目标入组 50 人开始时间: 2013年7月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) Anemia for other reasons than the renal anemia: 1) Iron deficiency (Serum ferritin <100 ng/mL and transferrin saturation <20%) 2) Vitamin B12 deficiency 3) Folic acid deficiency 4) Apparent hemorrhagic lesion 5) hematologic disease (e.g. leukemia, malignant lymphoma, myelodysplastic syndrome, aplastic anemia) 6) Disease associated with chronic inflammation (e.g. rheumatoid arthritis, inflammatory bowel disease) 7) Under myelosuppressive therapy (immunosuppressive therapy, chemotherapy or radiotherapy) (2) Under treatment for malignansy and severe infection (3) Post renal transplant patient (4) Hypersensitivity to epoetin beta pegol (5) Pregnancy or lactating (6) eGFR <6.0 mL/min/1.73 m2

研究者

发起方
Toda Central General Hospital

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