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临床试验/NL-OMON33255
NL-OMON33255已完成不适用

A Multi-Center Study Combined Non-Invasive Coronary Angiography and Myocardial Perfusion Imaging Using 320 Detector Computed Tomography - Coronary Angiography and Myocardial Perfusion with 320 Detector CT

Toshiba Medical Systems0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Male or female patients, age 45-85. ;Suspected or diagnosed coronary artery disease with a clinical indication for coronary angiography; and planned coronary angiography within the next 60 days.;Able to understand and willing to sign the Informed Consent Form.

排除标准

  • Known allergy to iodinated contrast media;History of contrast-induced nephropathy;History of multiple myeloma or previous organ transplantation;Elevated serum creatinine OR calculated creatinine clearance of <60 ml/min;Atrial fibrillation or uncontrolled tachyarrhythmia, or advanced atrioventricular block (second or third degree heart block);Evidence of severe symptomatic heart failure (NYHA Class III or IV); Known or suspected moderate or severe aortic stenosis ;Previous cardiac surgery;Coronary artery intervention within the last 6 months ;Known or suspected intolerance or contraindication to beta-blockers including;Severe pulmonary disease (chronic obstructive pulmonary disease)

研究者

发起方
Toshiba Medical Systems

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