Predictors for Recurrence of Atrial Fibrillation After Electrical Cardioversion (PRE-ELECTRIC)
In patients with persistent atrial fibrillation (AF), electrical cardioversion is very effective in restoring sinus rhythm if modern, biphasic cardioverters are used. However, approximately 50 per cent of the successfully cardioverted patients experience a recurrence of AF within a few weeks. Therefore, valid predictors for AF recurrence would be of great clinical relevance, to avoid unnecessary procedures.
In the PRE-ELECTRIC study, we will investigate the predictive value of potential new biomarkers with respect to AF recurrence within 30 days after electrical cardioversion. We will investigate serum and plasma biomarkers, electrocardiological markers and echocardiographic variables in this respect. The study will be undertaken as a prospective cohort study at Bærum Hospital, Vestre Viken Hospital Trust, with national and international collaborators.
研究概览
地位
条件
研究类型
注册 (预期的)
联系人和位置
学习联系方式
- 姓名:Arnljot Tveit, MD, PhD
- 电话号码:0047-97171773
- 邮箱:arnljot.tveit@vestreviken.no
研究联系人备份
- 姓名:Mona Olufsen, RN
- 电话号码:0047-90637441
- 邮箱:mona.olufsen@vestreviken.no
学习地点
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Bærum
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Sandvika、Bærum、挪威、1346
- 招聘中
- Bærum Hospital, Vestre Viken
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接触:
- Arnljot Tveit, MD, PhD
- 电话号码:0047-97171773
- 邮箱:arnljot.tveit@vestreviken.no
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接触:
- Elizabeth Lyster Andersen, MD
- 电话号码:0047-90882242
- 邮箱:ellyan@vestreviken.no
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Patients > 18 years referred for electrical cardioversion for persistent atrial fibrillation
- Signed, informed consent
Exclusion Criteria:
- Patients < 18 years
- Patients with paroxysmal atrial fibrillation
- Patients unwilling to participate or without consent competence
学习计划
研究是如何设计的?
设计细节
- 观测模型:队列
- 时间观点:预期
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Atrial fibrillation recurrence
大体时间:30 days after electrical cardioversion
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ECG-documented atrial fibrillation recurrence after successful cardioversion
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30 days after electrical cardioversion
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.