EUCTR2014-000269-27-DE进行中(未招募)不适用
Efficacy and tolerance of Beta Blocker and Procoralan uptitration in chronic heart failure patients under telemedical control: „70 bpm on day 28 - EARLY
German Foundation for Chronically Ill0 个研究点开始时间: 2014年6月23日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •Symptomatic heart failure with reduced left ventricular function caused by dilated cardiomyopathy (DCM) or ischemic cardiomyopathy (ICMP)
- •Heart rate = 75 bpm
- •NYHA Class II-IV
- •Sinus rhythm
- •Cognitive capacity
- •Age = 18 years
- •Stable HF medication including beta-blocker
- •Dose of beta-blocker = 50% of advised dose according to German product information or beta-blocker naive patient
- •Signed informed consent
- •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 70
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •Systolic blood pressure < 95 mm Hg
- •Cardiac decompensation within the last 8 weeks prior to recruitment
- •Significantly reduced renal function (GFR < 30)
- •Planned invasive medical intervention within the next 8 weeks
- •Lack of communication skills
- •Permanent atrial fibrillation and/or paroxysmal AF documented in two ECGs
- •Implanted active CRT-Device or active pacemaker
- •Patients with a contraindication for beta-blocker therapy
- •Patients under current Ivabradine-therapy
- •Patients paticipats in a competing clinical trial (identical/overlapping) inclusion criteria
- •Patients living in a geographic region without sufficient cell network coverage
研究者
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