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临床试验/DRKS00027420
DRKS00027420尚未招募不适用

Study of atrial fibrillation-burden and -pattern in patients with implanted device

niversitätsklinikum Essen0 个研究点目标入组 50 人开始时间: 2023年3月20日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50

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 Years 至 one(—)
性别
All

入选标准

  • 1) Patients with a BIOTRONIK dual-chamber ICD, DX, CRT-D, CRT-P, or pacemaker
  • 2) Inclusion no earlier than 4 weeks after implantation
  • 3) Patients's agreement to use CardioMessenger® and BIOTRONIK Home Monitoring®
  • 4) Age = 18 years
  • 1st group: Documented paroxysmal or persistent atrial fibrillation and increased NT-pro-BNP (> 125pg / ml) within the last 8 weeks
  • 2nd group: Sinus rhythm and CHA2DS2VASc value = 4 or sinus rhythm and increased NT-proBNP (> 125pg / ml) within the last 8 weeks

排除标准

  • 1. Life expectancy <1 year
  • 2. Inability of the patient to complete the study protocol
  • 3. Known alcohol or drug addiction
  • 4. Participation in another interventional clinical study
  • 5. Existing or currently planned pregnancy

研究者

发起方
niversitätsklinikum Essen

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