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临床试验/NCT05342220
NCT05342220已完成不适用

Effect of Ischemic Preconditioning on Relapse of Nonvalvular Atrial Fibrillation After Electrocardioversion

St. Josefs-Hospital Wiesbaden GmbH1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2022年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
240
试验地点
1
主要终点
Number of subjects with recurrence of atrial fibrillation 30 days after electrical cardioversion

研究概览

简要总结

Remote ischemic preconditioning is one way to influence the success of therapy in cardiovascular patients. By means of remote ischemic preconditioning the incidence of atrial fibrillation after cardiac surgery was reduced by 54%. The investigators aim to investigate the effect of ischemic preconditioning in an easy-to-perform protocol with regard to the recurrence of atrial fibrillation after electrical cardioversion.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with paroxysmal or persistent atrial fibrillation who give written informed consent to participate in the study
  • •Age > 18 years
  • •Consent capacity

排除标准

  • •Age under 18 years
  • •Pregnancy
  • •Lack of consent capacity

研究组 & 干预措施

Control

Sham Comparator

Sham preconditioning

干预措施: Sham preconditioning (Procedure)

Remote Ischemic Preconditioning

Active Comparator

Remote ischemic preconditioining

干预措施: Remote ischemic preconditioning (Procedure)

结局指标

主要结局

Number of subjects with recurrence of atrial fibrillation 30 days after electrical cardioversion

时间窗: 30 days

次要结局

  • Cumulative number of shocks delivered for successfull electrocardioversion(30 days)
  • Minimum energy required for successful electrocardioversion (in Joule)(30 days)
  • Cumulative energy applied for successfull electrocardioversion (in Joule)(30 days)
  • Number of patients with short-term cardioversion success(30 seconds)
  • Number of patients experiencing death from any cause, stroke /transient ischemic attack, relevant post-ECV arrhythmia and procedure-associated complications(30 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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