EUCTR2018-000889-11-NO进行中（未招募）1 期
Randomized Evaluation of Beta Blocker and ACE-Inhibitor/Angiotensin Receptor Blocker Treatment in MINOCA patients - MINOCA-BAT - MINOCA-BAT
Department of Medical Sciences, Akademiska sjukhuset0 个研究点目标入组 3,500 人开始时间: 2020年8月25日最近更新:
适应症
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
- 3,500
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.Age >18 years.
- •2.A clinical diagnosis of MINOCA within the last 30 days.
- •3.Left ventricular ejection fraction =40% measured with echocardiography, MRI or left ventriculography during hospitalization and prior to randomization.
- •4.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 20
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •1.Any condition that may influence the patient's ability to comply with study protocol.
- •2.Previous revascularization (CABG or PCI)
- •3.Clinical signs of heart failure
- •4.MRI-proven myocarditis or a strong clinical suspicion of myocarditis as cause of the index event
- •5.Contraindications for beta-blockade
- •6.Contraindications for ACEI and ARB
- •7.Prior use of ACE-I, ARB, or beta blockers, which must continue according to treating physician.
- •8.New indication for beta-blockade or ACEI/ARB other than as secondary prevention according the investigator
- •9.Ongoing pregnancy or woman of childbearing potential not using highly effective contraceptives
- •9.Participation in a trial evaluating a drug known to interact with beta blockers or ACEI/ARB
研究者
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