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首页> 外文期刊>Trials >Mobile phones in cryptogenic strOke patients Bringing sIngle Lead ECGs for Atrial Fibrillation detection (MOBILE-AF): study protocol for a randomised controlled trial
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Mobile phones in cryptogenic strOke patients Bringing sIngle Lead ECGs for Atrial Fibrillation detection (MOBILE-AF): study protocol for a randomised controlled trial

机译:隐源性卒中患者的手机携带单导铅心电图进行房颤检测(MOBILE-AF):一项随机对照试验的研究方案

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摘要

Background Recently published randomised clinical trials indicate that prolonged electrocardiom (ECG) monitoring might enhance the detection of paroxysmal atrial fibrillation (AF) in cryptogenic stroke or transient ischaemic attack (TIA) patients. A device that might be suitable for prolonged ECG monitoring is a smartphone-compatible ECG device (Kardia Mobile, Alivecor, San Francisco, CA, USA) that allows the patient to record a single-lead ECG without the presence of trained health care staff. The MOBILE-AF trial will investigate the effectiveness of the ECG device for AF detection in patients with cryptogenic stroke or TIA. In this paper, the rationale and design of the MOBILE-AF trial is presented. Methods For this international, multicentre trial, 200 patients with cryptogenic stroke or TIA will be randomised. One hundred patients will receive the ECG device and will be asked to record their ECG twice daily during a period of 1?year. One hundred patients will receive a 7-day Holter monitor. Discussion The primary outcome of this study is the percentage of patients in which AF is detected in the first year after the index ischaemic stroke or TIA. Secondary outcomes include markers for AF prediction, orally administered anticoagulation therapy changes, as well as the incidence of recurrent stroke and major bleeds. First results can be expected in mid-2019. Trial registration ClinicalTrials.gov, ID: NCT02507986 . Registered on 15 July 2015.
机译:背景技术最近发表的随机临床试验表明,对隐源性卒中或短暂性脑缺血发作(TIA)患者,延长的心电图(ECG)监测可能会增强对阵发性心房颤动(AF)的检测。一种可能适合长时间ECG监测的设备是与智能手机兼容的ECG设备(Kardia Mobile,Alivecor,旧金山,加利福尼亚州,美国),它使患者无需训练有素的医护人员就可以记录单导联ECG。 MOBILE-AF试验将研究ECG装置在患有隐源性卒中或TIA的患者中进行AF检测的有效性。本文介绍了MOBILE-AF试验的原理和设计。方法在这项国际性的多中心试验中,将随机分组200名隐源性卒中或TIA患者。一百名患者将使用ECG设备,并被要求在1年内每天两次记录其ECG。一百名患者将接受为期7天的动态心电监护仪。讨论这项研究的主要结果是在指数性缺血性卒中或TIA后的第一年内检测到房颤的患者百分比。次要结果包括房颤预测的标志物,口服抗凝治疗方法的改变以及复发性中风和大出血的发生率。预计将于2019年中期取得首个结果。试用注册ClinicalTrials.gov,ID:NCT02507986。 2015年7月15日注册。

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