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临床试验/EUCTR2005-000087-12-IT
EUCTR2005-000087-12-IT进行中(未招募)不适用

A multicentre, randomised, double-blind, parallel group, phase IV study to compare the renal effects of the non-ionic iso-osmolar contrast medium, iodixanol 320 mg I/mL VisipaqueTM , with the non-ionic low osmolar contrast medium, iopamidol 300 mg I/mL, in subjects with impaired renal function and diabetes mellitus undergoing multidetector-row helical CT

AMERSHAM HEALTH0 个研究点目标入组 500 人开始时间: 2007年1月19日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 未提供

研究者

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