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临床试验/ISRCTN17213748
ISRCTN17213748已完成未知

Efficacy of DE-MRI-guided fibrosis ablation vs. conventional Catheter Ablation of Atrial Fibrillation: DECAAF II

St Jude Medical0 个研究点目标入组 900 人开始时间: 2015年12月8日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
900

研究概览

简要总结

2021 Protocol article in https://pubmed.ncbi.nlm.nih.gov/33600025/ (added 13/01/2022)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Patients with persistent AF defined as 7 days or more of AF as evidenced by either:
  • 1.1 rhythm strip or
  • 1.2. written documentation
  • 2. Undergoing first AF ablation as per recent HRS consensus document (has not had a previous left atrial ablation or cardiac surgical procedure)
  • 3. Age = 18 years

排除标准

  • 1. Contraindication for DE-MRI with a full dose of contrast agent
  • 2. Contraindication to beta blockers, if necessary, for DE-MRI
  • 3. Women currently pregnant
  • 4. Mental or physical inability to take part in the study
  • 5. Inability to be placed in MRI due to body mass or body habitus
  • 6. Known terminally ill patients
  • 7. Subjects without daily access to a smart phone or tablet compatible with the ECG Check application and ability to upload ECG tracings for the entire follow up period.

研究者

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