EUCTR2014-004021-41-GB进行中(未招募)1 期
Prediction of Recurrent Events with 18F-Fluoride to Identify Ruptured and High-risk Coronary Artery Plaques in Patients with Myocardial Infarction - the PREFFIR study - PREFFIR - Prediction of Recurrent Events With 18F-Fluoride
niversity of Edinburgh0 个研究点目标入组 700 人开始时间: 2015年4月21日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 700
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
- •1.Patients aged =50 years with recent (<21 days) type 1 myocardial infarction and angiographically proven multi-vessel coronary artery disease defined as at least two major epicardial vessels with any combination of either (a) >50% luminal stenosis, or (b) previous revascularization (percutaneous coronary intervention or coronary artery bypass graft surgery).
- •2.Provision of informed consent prior to any study specific procedures
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 300
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 400
排除标准
- •1. Inability or unwilling to give informed consent
- •2.Women who are pregnant, breastfeeding or of child-bearing potential (women who have experienced menarche, are pre-menopausal and have not been sterilised) will not be enrolled into the trial
- •3.Major intercurrent illness with life expectancy <2 year
- •4.Renal dysfunction (estimated glomerular filtration rate =30 mL/min/1.73 m2)
- •5.Contraindication to iodinated contrast agent, positron emission tomography or computed tomography
- •6.Permanent or persistent atrial fibrillation
- •7.Previous screening as part of the trial
研究者
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