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临床试验/NL-OMON47473
NL-OMON47473已完成4 期

Contrast Medium Reduction with AlluraClarity for Iliac/Peripheral and EVAR procedures - Contrast Medium Reduction with AlluraClarity (COMER)

Philips0 个研究点目标入组 260 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
Philips
入组人数
260

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
18 至 64(—)

入选标准

  • * Subject will be undergoing an EVAR or iliac/peripheral procedure
  • * Subject is 18 years of age or older

排除标准

  • * Subject with contrast allergies
  • * Subject with severe kidney disease (e-GFR<45, determined by the MDRD formula)
  • * Subject participates in a potentially confounding drug or device trial during the course of the study.
  • * Subject meets an exclusion criteria according to national law (e.g. age, pregnant woman, breast feeding woman)
  • * Subject with overt hyperthyroidism

研究者

发起方
Philips

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