EUCTR2015-004657-40-SE进行中（未招募）1 期
Minimizing contrast agent in computed tomography pulmonary angiography
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 55
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
- •- Age >= 40 years
- •- Referred for computed tomography concerning thorax/chest-abdomen, or similar
- •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 55
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 55
排除标准
- •- Referral including question of aortic dissection or aortic aneurysm.
- •- Previous hypersensitivity to iodinized contrast agent, CT-examination planned with prophylaxis against hypersensitivity reaction or clinical request to minimize contrast agent dose.
- •- Previous examination with iodinized contrast agent within the last 48 hours.
- •- CT-protocol selection for clinical series not suitable for combination with study protocol.
- •- Contrast agent dose for clinical series > 100 ml, or not suitable for combination with study protocol.
- •- Patient weight >85 kg.
- •- Estimated Glomerular Filtration Rate <60 ml/min.
- •- Serum or plasma creatinine test older than 24 hours (acute referral) / older than 3 months (non-acute referral/planned examinations).
- •- Patient requiring continous medical surveillance.
- •- Patient requiring interpreter or inable to follow breathing instructions for examination.
- •- Pregnant, potentially pregnant or nursing women, according to the patient.
- •- Patient unable to perform CT-examination with arms above the head or patient without periferal venous catheter in the arm.
- •- Thyrotoxicosis or Myastenia gravis
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