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临床试验/NL-OMON39821
NL-OMON39821已完成3 期

A multicenter, randomized, double-blind, parallel group, active-controlled study to evaluate the efficacy and safety of both aliskiren monotherapy and aliskiren/enalapril combination therapy compared to enalapril monotherapy, on morbidity and mortality in patients with chronic heart failure (NYHA Class II - IV) - Atmosphere

ovartis0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
ovartis
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • See protocol for complete criteria (page34)
  • 1. Out patients * 18 years of age, male or female.
  • 2. Patients with a diagnosis of chronic heart failure (NYHA Class II * IV):
  • * LVEF * 35% at visit 1 (local measurement, within the past 6 months).
  • * Elevated BNP at visit 1: BNP * 150 pg/ml (according to local measurement).
  • OR BNP * 100 pg/ml (according to local measurement) and unplanned
  • hospitalization with HF within the last 12 months prior visit 1.
  • Elevated NT-proBNP at visit 1: BNP * 600 pg/ml (according to local measurement).
  • OR NT-proBNP * 400 pg/ml (according to local measurement) and unplanned
  • hospitalization with HF within the last 12 months prior visit 1.;3. Patients must be treated with an ACE inhibitor at a stable dose (enalapril 10 mg
  • daily at least or any other ACE inhibitor based on equivalent doses described in
  • Table 4-1: Dose equivalence guidance table of ACEi's) for at least 4 weeks prior
  • to visit 1.
  • 4. Patients must be treated with a beta blocker, unless contraindicated or not
  • tolerated, at a stable dose for at least 4 weeks prior to visit 1 (for patients not
  • on target dose, according to local guidelines, or in absence of that medication,
  • the reason should be documented).

排除标准

  • See protocol for complete criteria (page34-36)
  • 2. Patients treated concomitantly with both ARB and aldosterone antagonist in
  • addition to study drug at visit 1.
  • 4. Symptomatic hypotension and/or less than 95 mmHg SBP at Visit 1 and/ or less
  • than 90 mmHg SBP at Visits 4.
  • 5. Acute coronary syndrome, stroke, transient ischemic attack, cardiac, carotid or
  • major vascular surgery, percutaneous coronary intervention (PCI) or carotid
  • angioplasty, within the past 3 months prior to visit 1.
  • 6. Coronary or carotid artery disease likely to require surgical or percutaneous
  • intervention within the 6 months after visit 1.
  • 18. Serum potassium * 5.0 mmol/L at Visit 1 or * 5.2 mmol/L at Visit 4.
  • 29. Patients with diabetes mellitus

研究者

发起方
ovartis

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