ACTRN12620001374954尚未招募未知
se of single lead ECG to assist cardioversion in atrial fibrillation in the Emergency department - a pilot study
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 50
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
- Non-randomised trial
- 主要目的
- Diagnosis
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •50 patients with AF onset less than 24 hours presenting to ED who are able to have delayed cardioversion.
- •Age: 18 years or greater
- •Residing within the Eastern Health catchment during the initial intervention period (48 hours from time of ED presentation)
- •Haemodynamically stable
- •Recent onset AF : <24 hours of symptomatic first episode or recurrent AF
- •Have compatible smart phone or tablet to use the Alivecor device
排除标准
- •AF onset time unclear.
- •History of long-standing persistent AF (continuous AF for more than 1 year)
- •Patients with haemodynamically unstable AF who require emergent cardioversion
- •Have a cardiac pacemaker or implantable cardioverter defribrillator or other implanted electronic device
- •Unable to provide informed consent
研究者
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