2025-523589-26-00招募中4 期
Infusion of Furosemide to Improve Diuretic Efficiency in Acute Heart Failure (INFUSE-AHF)
Region Midtjylland7 个研究点 分布在 1 个国家目标入组 436 人开始时间: 2026年5月1日最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 436
- 试验地点
- 7
- 主要终点
- Net weight loss 3 days (≈72 hours) after randomisation
研究概览
简要总结
To determine if there is a difference in the diuretic treatment effect in acute heart failure between intravenous administration of furosemide by either continuous infusion preceded by a loading dose or bolus injections three times a day.
研究设计
- 分配方式
- Na
- 主要目的
- Follow-up phase
- 盲法
- None
入排标准
- 年龄范围
- 18 years 至 65+ years(65+ Years, 18-64 Years)
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of acute heart failure with volume overload
- •≥ 1 sign of volume overload
- •Anticipated intravenous furosemide ≥ 3 days
- •Age ≥ 18 years
排除标准
- •Patient requiring treatment with inotropes or vasopressors
- •Current or planned use of renal replacement therapy or ultrafiltration
- •Patient with a renal transplant
- •Patients who are pregnant or breastfeeding
- •Severe hypokalaemia (<2.5 mmol/L) or severe hyponatremia (<125 mmol/L)
- •Allergy to furosemide and its components
研究组 & 干预措施
FUROSEMIDE
Test
干预措施: FUROSEMIDE (Drug)
结局指标
主要结局
Net weight loss 3 days (≈72 hours) after randomisation
Net weight loss 3 days (≈72 hours) after randomisation
次要结局
- Net weight loss 2 days (≈48 hours) after randomisation
- Change in dyspnea on a Visual Analogue Scale 3 days (≈72 hours) after randomisation
- Days alive out-of-hospital to Day 30
- Length of stay
研究者
Esben Merrild
Scientific
Region Midtjylland
研究点 (7)
Loading locations...
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