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Direct Left Ventricular Rapid Pacing Via the Valve Delivery Guide-wire in TAVI — EASY TAVI  

Aortic Valve Stenosis Clinical Trial

Official title:
Direct Left Ventricular Rapid Pacing Via the Valve Delivery Guide-wire in TAVI: a Randomized Study

Clinical Trial Summary

The purpose of this study is to determine whether a left ventricular rapid pacing using the valve delivery guide-wire in transcatheter aortic valve implantation (TAVI) reduces the overall procedure duration in comparison with the conventional method.

Clinical Trial Description

Use of temporary pacing via a right ventricular lead in TAVI is still mandatory to ensure transient cardiac standstill while predilatation is performed and the valve is being positioned and deployed. This requires an additional venous vascular access and a pacing catheter which are both likely to generate complications.

This study compares the standard right ventricular rapid pacing to a new and simplified technique : a left ventricular rapid pacing is provided via the back-up 0.035 " guidewire. The cathode of an external pacemaker is placed on the tip of the 0.035" wire and the anode on a needle inserted into the groin. Insulation is ensured by the balloon or TAVI catheter. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02781896
Study type Interventional
Source Groupe Hospitalier Mutualiste de Grenoble
Contact
Status Completed
Phase N/A
Start date May 12, 2017
Completion date June 29, 2018
View Details
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