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临床试验/NCT03614377
NCT03614377Unknown不适用

Prospective Multicenter Observation Study on the Association Between the Severity of Device-detected Sleep-disordered Breathing and the Risk of Cardiac Arrhythmic Events

Samsung Medical Center14 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2017年4月28日最近更新:
适应症

试验速览

阶段
不适用
入组人数
600
试验地点
14
主要终点
Number of participants with atrial fibrillation

研究概览

简要总结

This prospective multicenter registry study aims to determine whether device-detected sleep-disordered breathing events are associated increased risk of cardiac arrhythmias or other cardiovascular outcomes.

详细描述

The prevalence of SDB high in patients with cardiac implantable electronic device (CIED). Recently, device-detected SDB events showed a correlation with sleep-disordered breathing (SDB) diagnosed by polysomnography. Thus, CIED will facilitate early detection and monitoring of SDB in patients with CIEDs. Few studies investigated prognostic value of CIED-detected SDB in risk of cardiovascular events. Therefore, the primary aim is to determine whether device-detected SDB are associated with increased risk of cardiac arrhythmias or other cardiovascular morbidities using a prospective multicenter registry.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age ≥ 19years
  • CHA2DS2VASc score ≥ 1 in male or ≥ 2 in female

排除标准

  • CIED without atrial lead
  • persistent or permanent atrial fibrillation (AF) or flutter
  • history of catheter of surgical ablation of AF
  • valvular steno-insufficiency more than moderate degree
  • chronic obstructive pulmonary disease
  • under current treatment for sleep-disordered breathing
  • life expectancy < 1year

结局指标

主要结局

Number of participants with atrial fibrillation

时间窗: from enrollment to last follow-up (2 years)

cardiac implantable electronic device-detected or clinical atrial fibrillation

次要结局

  • Number of participants with ventricular arrhythmia(from enrollment to last follow-up (2 years))
  • Number of participants with complications associated with atrial fibrillation(from enrollment to last follow-up (2 years))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (14)

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