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临床试验/NL-OMON50896
NL-OMON50896招募中不适用

The effectivity of lifestyle interventions and prevention in patients with atrial fibrillation referred for ablation; a randomised-controlled trial - Prevention to improve Outcomes after PVI (POP-trial)

Catharina-ziekenhuis0 个研究点目标入组 150 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
招募中
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Patients with paroxysmal or persistent atrial fibrillation referred for initial
  • catheter ablation
  • Age 18-75 years
  • The patient should have at least on treatable risk factor (BMI >=27 kg/m2,
  • hyperlipidaemia, hypertension, diabetes mellitus with HbA1c >=53 mmol/mol,
  • active smoking, or excess alcohol use)
  • Patients are willing and able to use the VitalHealth Engage platform on their
  • own preferred device

排除标准

  • Longstanding persistent atrial fibrillation (persistent atrial fibrillation for
  • more than 1 year)
  • Permanent atrial fibrillation
  • Asymptomatic atrial fibrillation
  • Prior ablation
  • Severe valvular heart disease
  • Prior or soon foreseen implantation of cardiac device
  • Acute coronary syndroom < 3 months before inclusion
  • Unstable heart failure NYHA IV or heart failure necessitating admission <3
  • months before inclusion
  • Cardia surgery <3 months before inclusion
  • Life expectancy <1 year

研究者

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