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More info
You can access this
clinical trial
if you have
Atrial Fibrillation, Atrial Fibrillation Ablation or Pulmonary Vein Isolation
and you are
between 18 and 85
years old
-
The phase for this study is not defined.
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The purpose

The most widely used approach for the invasive treatment of paroxysmal atrial fibrillation is catheter ablation, by which radiofrequency energy is used to heat the tip of an ablation catheter to deliver targeted burns on the inner surface of the heart. The aim of this approach is to cause electrical isolation of the pulmonary veins. The purpose of this study is to evaluate whether the information which can be derived from the latest catheter technologies - on the degree of contact force between the catheter and the heart - affects the time to perform the procedure, or the outcomes as a result of it. Patients undergoing pulmonary vein isolation will be randomised to having their procedure performed with the contact force information available to the operator, or not available. The time taken to achieve pulmonary vein isolation is the primary end-point of the study.

Provided treatments

  • Procedure: Pulmonary vein isolation using contact force sensing catheter

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01730924. The sponsor of the trial is Queen Mary University of London and it is looking for 120 volunteers for the current phase.
Official trial title:
A Randomised Study Comparing Pulmonary Vein Isolation Using SmartTouch® Catheter With or Without Real-time Contact Force Data. The SMART Trial