跳至主要内容
临床试验/EUCTR2014-004021-41-GB
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

发起方
niversity of Edinburgh

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