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临床试验/EUCTR2014-000269-27-DE
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

发起方
German Foundation for Chronically Ill

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