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临床试验/EUCTR2016-004193-18-HU
EUCTR2016-004193-18-HU进行中(未招募)1 期

Effect of repetitive levosimendan treatment on clinical outcomes of chronic heart failure patients: focus on optimal patient selection based on novel cardiac biomarkers.

Semmelweis University, Heart and Vascular Center0 个研究点开始时间: 2016年10月24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

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. Symptomatic heart failure at enrollment – NYHA III-IV treated with augmented / iv. diuretics with optimal heart failure medical treatment
  • 2. Ischaemic patients (no STEMI/ NSTEMI in 6 months) with a device specified as: Non reposponders or low responders after CRT-P/CRT-D or after ICD implantation (at least for 6 months)
  • 3. Ischaemic or non-ischaemic chronic heart failure without any device.
  • 4. Age: 18-80 years
  • 5. LVEF<35%
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 80

排除标准

  • SBP<100 Hgmm
  • AMI, stroke or life-threatening arrhytmia in the last 3 months
  • Multiorgan failure
  • Chronic kidney disease kreat >250
  • Severe COPD treated with steroid or more than 2 inh. therapy
  • Severe anaemia <100 mg/dl
  • GOT / GPT > 100 U/L
  • Any planned surgical event or TX
  • Non-consent or low compliant
  • Use of levosimendan in the patients’ history in the past 6 months

研究者

发起方
Semmelweis University, Heart and Vascular Center

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