IRCT20230809059099N2招募中Unknown
Efficacy and safety of the Defibrillator / Monitor model Re-pulse6 Avecinna Co. among patients with atrial fibrillation and flutter who are candidates of elective cardioversion: a stratified non-inferiority randomized controlled trial at Tehran Heart Center
Avecinna co0 个研究点目标入组 105 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 105
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 years 至 90 years（—）
- 性别
- All
入选标准
- •Age >18 years old
- •Atrial fibrillation or flutter
- •indication for cardioversion
- •Atrial fibrillation or flutter will be confirmed by an electrophysiologist using 12 lead standard ECG. Cardioversion will be conducted at the discretion of the electrophysiologist.
- •All patients are required to receive at least 4 weeks of antio coagulation or left atrial thrombus is ruled out by trans esophageal echocardiography
排除标准
- •Requiring emergeny cardioversion
- •Hemodynamic instability
- •Chest pain or suspicion of acute coronary syndrome
- •Hypokalemia
- •Digoxin toxicity
- •Pregnancy or breastfeeding
- •No informed consent
研究者
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