NL-OMON51987招募中不适用
Improving the Cost-effectiveness Of Coronary Artery Disease Diagnosis - iCORONARY
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 3,300
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
- •The subject is >= 18 years of age
- •The subject is willing and able to provide informed consent and adhere to
- •study rules and regulations and follow-up
- •The subject is clinically suspected of having (recurrent) angina pectoris or
- •an equivalent and suspected coronary artery disease, based on symptoms and
- •signs, history, clinical examination and baseline diagnostic testing (e.g. ECG
- •recording and laboratory tests) as described in the 2019 ESC guideline on
- •chronic coronary syndromes.
- •The subject has had >=64 multidetector row coronary CTA or agrees to undergo
- •coronary CTA with >=64 multidetector row coronary CTA.
排除标准
- •The subject has at least one coronary stenosis of >=90% diameter reduction as
- •seen on coronary CTA
- •The subject is suffering from unstable angina pectoris.
- •The subject is suffering from decompensated congestive cardiac failure.
- •The subject is suffering from a known non-ischemic cardiomyopathy.
- •The subject has a history of percutaneous coronary intervention or coronary
- •artery bypass grafting.
- •The subject has pacemaker- or internal defibrillator leads implanted.
- •The subject has a prosthetic heart valve.
- •There is a severe language barrier.
- •The subject participates in any other clinical trial that interferes with the
- •current study.
- •The subject*s clinical condition prohibiting subsequent interventional
- •therapy as indicated by the results of the imaging procedures.
- •The subject is or might be pregnant.
- •The subject does not comply or is not able to comply to the imaging
- •guidelines for the performance and acquisition of CCTA by the SCCT
研究者
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