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Clinical Trial Summary

In this randomized study, two energy sources for the ablation of AV nodal reentry tachycardia are compared: The standard technique of radiofrequency energy delivery is compared with the new approach of cryo-energy application.


Clinical Trial Description

The ablation of AV nodal reentry tachycardia with radiofrequency (RF) energy delivering catheters is a standard procedure and in experienced EP laboratories, the safety and efficacy of this approach is very high.

However, the potential complication of higher degree AV conduction block, requiring in some instances implantation of a pacemaker, is a major drawback of this approach.

We want to compare in this randomized study the safety and efficacy of standard RF ablation with the cryo-ablation technique. This relatively new technique is thought to offer more safety concerning higher degree AV conduction block. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Atrioventricular Nodal Reentry Tachycardia
  • Tachycardia
  • Tachycardia, Atrioventricular Nodal Reentry

NCT number NCT00196222
Study type Interventional
Source Deutsches Herzzentrum Muenchen
Contact
Status Completed
Phase Phase 4
Start date March 2003
Completion date May 2009

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05705297 - Intracardiac Echocardiography Guided Slow Pathway Cryoablation
Recruiting NCT05296954 - Localization of Anatomical Structures Involved in Nodal Tachycardias by High Density Mapping. N/A
Completed NCT00875914 - Magnetically Navigated vs. Manually Guided Radiofrequency in Atrioventricular-node-reentry-tachycardia Phase 4