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临床试验/CTRI/2016/11/007459
CTRI/2016/11/007459已完成4 期

Effect of oral liposomal iron versus intravenous carboxymaltose iron for treatment of iron deficiency anaemia in CKD patients:a randomized trial

CBCI society for medical education0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方

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

入选标准

  • Age 18-65 years, Estimated glomerular filtration rate (eGFR, Modification of Diet in Renal Disease equation) <=60 mL/min/1.73 m2, Hb levels <=12 g/dL,plasma ferritin levels <=100 ng/mL, transferrin saturation (TSAT) <=25%, parathormone (PTH) serum levels between 30and 300 pg/mL, according to the suggested values for kidney disease stage and calcium and phosphate plasma levels within their normal values (i.e. <10.5 and <4.5 mg/dL, respectively).

排除标准

  • includes high-sensitivity C-reactive protein (hsCRP) levels >=5 mg/L, presence of inflammatory, infectious disease or surgical interventions in the last 3 months,haematological disorders, bleeding or blood transfusions in the last 6 months, malignancies, treatment with immunosuppressive drugs, severe malnutrition, concomitant severe liver or CV disease, chronic alcohol or drug abuse within the past 6 months,known hepatitis B or C infection, pregnant or lactating women.
  • Pharmacological and non-pharmacological therapies will be prescribed to each patient to achieve the therapeutic targets in keeping with the current practice guidelines suggested by K/DOQI CKD for Stages 3â??5

研究者

发起方
CBCI society for medical education

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