ACTRN12616001188426终止4 期
A double blind, randoMIsed controlled cliNical trIal comparing the effect of treatment with oral MRA (spironolactone) versus placebo on the frequency and duration of atrIal fibrillation in patients with an implanted cardiac device in New Zealand: MINIMIZE-AF
适应症
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 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
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 19 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patients with an implanted cardiac device capable of recording the frequency and duration of AF events and with
- •evidence of AF or AHRE within the 6months
- •prior to recruitment will be eligible.
- •age >18 years (without childbearing
- •potential for women); with an implantable device capable of
- •AF or AHRE monitoring; and with device documented AF or AHRE (defined as AHRE >220 bpm for >2% of the time
- •or for > 5mins on at least one occasion) in the last 6months.
排除标准
- •Permanent AF,
- •Receiving AF suppression pacing
- •History of heart failure with indication for MRAs
- •A clinical indication for MRA or K+ sparing diuretic
- •Contraindication to MRA
- •Severe renal dysfunction
- •Sustained hyperkalaemia in the absence of reversible cause
研究者
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