ACTRN12619000793112
招募中
未知
Smart Phone based single lead ECGs versus traditional ambulatory Holter monitoring for definite diagnosis of cardiac arrhythmias in patients with symptomatic palpitations: a randomised controlled trial
Western Sydney Local Health District (WSLHD)0 个研究点目标入组 80 人2019年5月29日
概览
- 阶段
- 未知
- 干预措施
- 未指定
- 疾病 / 适应症
- 未指定
- 发起方
- Western Sydney Local Health District (WSLHD)
- 入组人数
- 80
- 状态
- 招募中
- 最后更新
- 6年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •1\.Patients aged greater than or equal to 18 years;
- •2\.Symptomatic palpitations in whom initial 12 lead ECG has failed to detect arrhythmia.
- •3\.At least two episodes of palpitations in the preceding 6 months;
- •4\.Have a smartphone and/or a smartwatch capable of running the Alivecor application.
排除标准
- •Patients will be excluded if they are:
- •1\.are unable or unwilling to provide informed consent;
- •2\.Patients in whom palpitations are known to have a physiologic such as anaemia, thyroid dysfunction, heart failure, or women who are pregnant or breast feeding;
- •3\.Concomitant illness, physical impairment or mental condition which in the opinion of the study team/ primary care physician could interfere with the conduct of the study including outcome assessments;
- •4\.Inability or unwillingness to provide written informed consent;
- •5\.Unable to complete study procedures;
- •6\.Medical illness with anticipated life expectancy \< 3 months;
- •7\.Responsible primary care or other responsible physician believes it is not appropriate to participate in the study.
- •8\.poor baseline sECG recording;
- •9\.Lack of understanding of how to record sECG after initial consultation.
结局指标
主要结局
未指定
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