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临床试验/NCT01060293
NCT01060293终止4 期

Comparison of High-dose Furosemide, Low-dose Furosemide, and the Combination of Low-dose Furosemide and Low-dose Dopamine in Patients With Acute Decompensated Heart Failure

Larissa University Hospital6 个研究点 分布在 2 个国家目标入组 161 人开始时间: 2009年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
发起方
入组人数
161
试验地点
6
主要终点
1-year mortality or rehospitalization (all-cause, cardiovascular, non-cardiovascular, and due to worsening heart failure).

研究概览

简要总结

The aim of this study is to compare the effects of 1) high-dose furosemide, 2) low-dose furosemide, and 3) low-dose furosemide combined with low-dose dopamine on diuresis, clinical status, renal function, electrolyte balance, length of stay, and 60-day post-discharge outcomes in patients hospitalized with acute decompensated heart failure.

详细描述

The aim of this study is to compare the effects of:

  1. high-dose furosemide (HDF, 40 mg furosemide bolus IV, followed by continuous IV infusion of 20 mg/h for a total of 8 hours),
  2. low-dose furosemide (LDF, 40 mg furosemide bolus IV, followed by continuous IV infusion of 5 mg/h furosemide for a total of 8 hours), and
  3. low-dose furosemide combined with low-dose dopamine (LDFD, 40 mg furosemide bolus IV, followed by continuous IV infusion of 5 mg/h furosemide plus 5μg/kg/min dopamine for a total of 8 hours) on diuresis, perceived dyspnea, renal function, electrolyte balance, total length of stay, and 60-day post-discharge outcomes in patients hospitalized with ADHF.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with New York Heart Association (NYHA) functional class IV heart failure according to the American Heart Association (AHA) classification, namely dyspnea on minimal exertion or rest dyspnea, orthopnea, and paroxysmal nocturnal dyspnea,
  • signs of congestion (third heart sound or pulmonary rales on physical examination),
  • pulmonary congestion on chest x-ray,
  • serum B-type natriuretic peptide levels > 400 pg/ml or NT-proBNP > 1500 pg/ml,
  • echocardiographic documentation of systolic or diastolic dysfunction,
  • age >18 years old,
  • on medical therapy with an ACE-inhibitor and/or a β-blocker,
  • experiencing an acute decompensation of known chronic HF,
  • baseline oxygen saturation <90% on admission arterial blood gas

排除标准

  • acute de novo HF;
  • severe renal failure (serum creatinine >200 μmol/L or GFR <30 ml/min/1.73m2)
  • admission systolic blood pressure <90 mm Hg;
  • severe valvular disease;
  • known adverse reactions to furosemide or dopamine;
  • HF secondary to congenital heart disease;
  • a scheduled procedure with a need for IV contrast dye;
  • a scheduled cardiac surgery within 6 months

研究组 & 干预措施

High-dose furosemide

Active Comparator

High-dose furosemide (HDF): 20 mg/h continuous IV administration for 8 hours

干预措施: High-dose furosemide (Drug)

Low-dose furosemide

Active Comparator

Low-dose furosemide (LDF): continuous IV administration of 5 mg/h furosemide

干预措施: Low-dose furosemide (Drug)

Low-dose furosemide combined with low-dose dopamine

Active Comparator

Low-dose furosemide combined with low-dose dopamine (LDFD): continuous IV administration of 5 mg/h furosemide combined with 5 μg/kg/min dopamine for a total of 8 hours

干预措施: Low-dose furosemide combined with low-dose dopamine (Drug)

结局指标

主要结局

1-year mortality or rehospitalization (all-cause, cardiovascular, non-cardiovascular, and due to worsening heart failure).

时间窗: 1-year

次要结局

  • 60-day mortality or rehospitalization (all-cause, cardiovascular, non-cardiovascular, and due to worsening heart failure).(60-day post discharge)
  • Novel indices of acute renal ischemia/injury (cystatin-C, KIM-1, NGAL)(Throughout hospitalization)

研究者

发起方
Larissa University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gregory Giamouzis

Assistant Professor of Cardiology

Larissa University Hospital

研究点 (6)

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