跳至主要内容
临床试验/NL-OMON37262
NL-OMON37262已完成不适用

Determining Accuracy and Trending Characterization of AF - DETECT AF

St. Jude Medical0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - The subject has been implanted with a SJM Confirm ICM, DM2102.
  • - The subject has or is suspected to have paroxysmal AF.
  • - The subject is * 18 years of age.
  • - The subject is willing and able to provide written Informed Consent (prior to any
  • investigational related procedure).

排除标准

  • - The subject has persistent (>7 days and <1 year or AF requiring cardioversion),
  • longstanding persistent (continuous AF >1 year) or permanent AF (not attempting to
  • restore sinus rhythm).
  • - The subject has AF of reversible etiology (e.g. electrolyte imbalance, thyroid disease).
  • - The subject has a contraindication to Holter recording.
  • - The subject has already received an active implantable medical device other than the
  • SJM Confirm ICM, DM2102.
  • - The subject is unable to comply with the follow up schedule.
  • - The subject is participating in another investigational device or drug investigation.
  • - The subject is pregnant or is planning to become pregnant during the duration of the
  • investigation.

研究者

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