EUCTR2017-002336-17-EE进行中（未招募）1 期
Randomized Evaluation of Decreased Usage of betablocCkErs after myocardial infarction in the SWEDEHEART registry - REDUCe SWEDEHEART
Department of Clinical Sciences, Danderyd Hospital, Karolinska Intitutet0 个研究点目标入组 7,000 人开始时间: 2019年1月21日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 7,000
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
入选标准
- •1.Age = 18 years.
- •2.Day 1-7 after MI as defined by the universal definition of MI, type 1, included in the SWEDEHEART registry.
- •3.Coronary angiography performed during hospitalization.
- •4.Obstructive coronary artery disease documented by coronary angiography, i.e. stenosis = 50 %, FFR = 0.80 or iFR = 0.89 in any segment at any time point before randomization.
- •5.Echocardiography performed after the MI showing a normal ejection fraction (EF=50%).
- •6.Written informed consent obtained
- •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 3500
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 3500
排除标准
- •1.Any condition that may influence the patient’s ability to comply with study protocol.
- •2.Contraindications for beta-blockade
- •3.Indication for beta-blockade other than as secondary prevention according to the treating physician
- •Thus, use of oral beta-blockade on admission is not per se an exclusion criterion.
研究者
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