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临床试验/NCT00196170
NCT00196170Unknown4 期

Multicenter Prospective Randomized Clinical Study Comparing Radiofrequency- vs. Cryo-Ablation in Typical Isthmus-Dependent Atrial Flutter

Deutsches Herzzentrum Muenchen4 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2003年5月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
发起方
入组人数
500
试验地点
4
主要终点
Acute Efficacy (bidirectional cavotricuspid isthmus block)

研究概览

简要总结

This randomized study compares two energy sources for the catheter based ablation of typical isthmus-dependent atrial flutter: The (standard) radiofrequency (RF) ablation technique and the cryo-ablation technique regarding the acute and long term efficacy and safety.

详细描述

This randomized study compares two energy sources for the catheter based ablation of typical isthmus-dependent atrial flutter: The (standard) radiofrequency (RF) ablation technique and the cryo-ablation technique. The RF ablation of typical atrial flutter has become a standard approach with very high curing rates and low complication incidence. However, ablation with RF is painful since the underlying cardiac tissue heats up (up to 70-80°C inside the tissue) and especially the target of ablation in typical atrial flutter, the so-called cavo-tricuspid isthmus, is a very pain-receptive area. Cryo-ablation, which destroys tissue by freezing it down to -80 to -90°C, is thought to be less painful or even painless with the same efficacy than RF ablation.

The acute and long term (6 months follow-up, non-invasive) efficacy and safety is the combined endpoint.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •age between 18 and 80 years
  • •documented atrial flutter which is most probably typical isthmus dependent atrial flutter
  • •informed written consent

排除标准

  • •prior ablation for atrial flutter
  • •concomitant arrhythmia which is treated during the same ablation procedure
  • •prior MAZE operation
  • •contra indication for catheterization
  • •physical or psychiatric disorder making participation in the study impossible
  • •pregnancy
  • •prior participation in the study
  • •participation in another study

研究组 & 干预措施

1

Experimental

8mm tip ablation catheter for ablation of cavotricuspid isthmus

干预措施: RF ablation of the cavo-tricuspid isthmus (Procedure)

2

Experimental

irrigated tip ablation catheter for ablation of cavotricuspid isthmus

干预措施: irrigated tip radiofrequency ablation of the cavo-tricuspid isthmus (Procedure)

3

Experimental

cryo 10mm tip ablation catheter for ablation of cavotricuspid isthmus

干预措施: cryo ablation of the cavo-tricuspid isthmus (Procedure)

4

Experimental

Cryo 6.5mm tip ablation catheter for ablation of cavotricuspid isthmus

干预措施: cryo 6.5mm tip ablation of the cavotricuspid isthmus (Procedure)

结局指标

主要结局

Acute Efficacy (bidirectional cavotricuspid isthmus block)

时间窗: bidirectional cavotricuspid isthmus block

Long-term efficacy (6 months FU freedom of typical atrial flutter)

时间窗: 6 months

Mortality

时间窗: 6 months

次要结局

  • Patients' pain scores during ablation(while hospitalisation)
  • Safety of ablational devices(6 months)

研究者

发起方
Deutsches Herzzentrum Muenchen
申办方类型
Other

研究点 (4)

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