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
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
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