跳至主要内容
临床试验/NCT01058551
NCT01058551已完成不适用

Incidence of New Onset Atrial Fibrillation in Patients With Severe Obstructive Sleep Apnea: The Reveal XT-SA Study

Dr. Adrian Baranchuk2 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2011年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
31
试验地点
2
主要终点
To determine the incidence of new onset AF in patient's with severe OSA

研究概览

简要总结

Single site study: The goal of the study is to determine the incidence of new onset atrial fibrillation (AF) in patients with severe obstructive sleep apnea (OSA) syndrome through the use of a Medtronic Reveal XT implantable Loop recorder (ILR). The ILR device is approved for use in Canada, for the assessment of atrial fibrillation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Patients with severe OSA defined as Apnea Hypopnea Index (AHI) >
  • Age > 18 years.

排除标准

  • Previous history of clinical AF defined as documented lone, paroxysmal, persistent or permanent, according to standard definitions.
  • Patient with anticipated requirement of MRI.
  • Patient with well-know allergy to any component of the Medtronic Reveal XT.
  • Patients with implantable cardiac rhythm device [pacemakers or internal cardiac device (ICDs)].
  • Women of child bearing potential.
  • Unable or unwilling to provide written informed consent.
  • Unable or unwilling to complete the study follow-up schedule (eg. intention to leave the Kingston area over the next 3 years.
  • Previously enrolled in this trial.
  • Enrolled in another study that would confound the results of this trial.
  • Documented history of heart failure
  • Diagnosed with severe obstructive sleep apnea greater than 1 year from screening date

结局指标

主要结局

To determine the incidence of new onset AF in patient's with severe OSA

时间窗: 36 months

次要结局

  • To determine the impact of continuous positive airway pressure (CPAP) treatment in patients with new onset of AF in patients with severe OSA. (post hoc analysis)(36 months)

研究者

发起方
Dr. Adrian Baranchuk
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr. Adrian Baranchuk

MD

Queen's University

研究点 (2)

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