跳至主要内容
临床试验/NL-OMON37797
NL-OMON37797尚未招募4 期

Effects of vernakalant and flecainide on atrial contractility in patients with atrial fibrillation - Vernakalant versus flecainide: atrial contractility

Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
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
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - patients presenting with paroxysmal or persistent AF;- eligible for treatment with flecainide or vernakalant infusion to restore sinus rhythm;- receiving adequate anticoagulant therapy (or having an episode of AF lasting < 24 hours)

排除标准

  • - atrial flutter;- contra-indications for receiving flecainide or vernakalant infusion according to MUMC+ protocol (unstable hemodynamic condition, LVEF < 40%, inadequate potassium levels, acute ischaemia, sinus node dysfunction);- age < 18 years

研究者

发起方
Medisch Universitair Ziekenhuis Maastricht

相似试验