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临床试验/NCT01997892
NCT01997892已完成不适用

TRANSFORM - Observational Cohort Study of Aranesp Use in EU Haemodialysis Patients Switched From Mircera

Amgen1 个研究点 分布在 1 个国家目标入组 1,027 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Amgen
入组人数
1,027
试验地点
1
主要终点
Hemoglobin Concentration at Monthly Intervals

研究概览

简要总结

To describe the time course of hemoglobin concentration in EU hemodialysis patients switched from methoxy polyethylene glycol-epoetin beta (PEG epoetin beta; Mircera) to darbepoetin alfa (Aranesp).

详细描述

This is a multi-centre, observational cohort study of EU hemodialysis patients whose erythropoiesis stimulating agent (ESA) therapy has been switched from PEG epoetin beta to darbepoetin alfa. Data will be collected for the period spanning 14 weeks prior to switch through to 26 weeks post-switch.

研究设计

研究类型
Observational
观察模型
Cohort

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients >18 years of age. CKD diagnosis, receiving hemodialysis
  • Received PEG epoetin beta for 14weeks prior to switching to darbepoetin alfa and received at least one dose of darbepoetin alfa.

排除标准

  • 未提供

结局指标

主要结局

Hemoglobin Concentration at Monthly Intervals

时间窗: Month -3, -2, -1 (pre-switch), and Month 1, 2, 3, 4, 5 and 6 (post-switch)

Hemoglobin concentration from 3 months prior to switch to darbepoetin alfa until the end of the observation period.

次要结局

  • PEG Epoetin Beta Dose From the Start of the Observation Period Until the Switch(Month -3, Month -2, Month -1)
  • Darbepoetin Alfa Dose From the Switch Date Until the End of the Observation Period(Month 1, 2, 3, 4, 5 and 6)
  • Dose Ratio Measured at the Time of Switch From PEG Epoetin Beta to Darbepoetin Alfa(Week -1 and Week 1)
  • Hemoglobin Concentration Rate of Change by Period(Thre months prior to switch and 6 months after the switch)
  • Percentage of Participants With Hemoglobin Excursions(Month -3, -2, -1, 1, 2, 3, 4, 5 and 6)

研究者

发起方
Amgen
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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