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临床试验/NCT00392431
NCT00392431已完成不适用

Continuous Versus Episodic Prophylactic Treatment With Oral Amiodarone for the Prevention of Permanent Atrial Fibrillation: a Randomized Study on Morbidity and Quality of Life

University Medical Center Groningen2 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2003年1月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
220
试验地点
2
主要终点
Adverse events related to amiodarone use and/or atrial fibrillation itself or underlying heart disease

研究概览

简要总结

Our hypothesis is that episodic amiodarone treatment (i.e. amiodarone treatment 1 month prior until 1 month after cardioversion) is associated with a lower morbidity and a higher quality of life compared to continuous prophylactic amiodarone treatment while atrial fibrillation is still effectively suppressed. The latter means that at the end of the study permanent atrial fibrillation is prevented in comparable percentage of patients (70%) in both treatment strategies. However, this will be accomplished at the cost of a higher number of electrical cardioversions (2-3) in the episodic treatment group compared to the continuous treatment group.

详细描述

Primary objective

To determine differences in adverse event rates between patients with persistent atrial fibrillation who are randomized to episodic amiodarone treatment (EAT) strategy and patients who are randomized to continuous amiodarone treatment (CAT) strategy, while atrial fibrillation is still effectively suppressed.

Adverse events can be related to:

  1. amiodarone use
  2. atrial fibrillation itself or underlying heart disease.

Secondary objective

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
None

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Adverse events related to amiodarone use and/or atrial fibrillation itself or underlying heart disease

次要结局

  • Quality of life
  • Number of patients with permanent AF at the end of the study

研究者

申办方类型
Other

研究点 (2)

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