跳至主要内容
临床试验/EUCTR2006-001298-57-BE
EUCTR2006-001298-57-BE进行中(未招募)不适用

Comparison of the diagnostic efficacy of Xenetix 350 and Iomeron 400, for visualisation of the aorta and abdominal vascular tree with 64-slices computed tomography

GUERBET0 个研究点目标入组 310 人开始时间: 2006年10月18日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
GUERBET
入组人数
310

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

  • - Male or female having reached legal majority age and up to 85 years included.
  • - Patient scheduled for an aorta and abdominal arterial tree evaluation by MSCT, either for pretherapeutic evaluation or for post-surgical control or follow-up (including patients with prosthetic vascular material).
  • - Female of childbearing potential must have effective contraception (contraceptive pill or Intra-Uterine Device), or be surgically sterilised, or post-menopausal (minimum 12 months amenorrhea) or must have a documented negative urine and/or blood pregnancy test at screening.
  • 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

  • - Patient with overt compensated heart failure.
  • - Patient with hemodynamic instability.
  • - Patient with ESC/ESH grade 3 hypertension.
  • - Patient with known renal failure.
  • - Patient who have received diuretic or biguanide treatment during the 48 hours preceding the MSCT scan.

研究者

发起方
GUERBET

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