NCT01415414已完成不适用
The Image Quality and Radiation Dose of CECT With Ultravist® in Patients With Abdominal Pelvic Disease - INDEX
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Bayer
- 入组人数
- 11,660
- 主要终点
- Image quality evaluated by calculated CNR (Contrast to Noise Ratio)
研究概览
简要总结
It is a prospective, non-interventional, multi-center study. The primary objective of this study is to evaluate the image quality of Ultravist in patients requiring contrast-enhanced CT considering the routine use in patient population's, region's indication.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients undergoing contrast enhanced CT Imaging with Ultravist (iopromide) in abdomen or pelvis.
排除标准
- •There is no other exclusion criteria beyond the contraindications contained in the Summary of Product Characteristics
研究组 & 干预措施
Group 1
干预措施: Iopromide (Ultravist, BAY86-4877) (Drug)
结局指标
主要结局
Image quality evaluated by calculated CNR (Contrast to Noise Ratio)
时间窗: 1 day
次要结局
- Image quality evaluated by calculated SNR (Signal Noise Ratio)(1 day)
- Radiation dose (CTDIvol)(1 day)
- Descriptive analysis of contrast medial injection protocol(1 day)
研究者
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