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Ultrasound-guided Axillary Vein Access Versus Cephalic Venous Cutdown for Implantation of Cardiac Electronic Devices.

Pacemaker Clinical Trial

Official title:
Prospective Randomized Comparison of Efficacy and Safety of Ultrasound-guided Axillary Vein Access Versus Cephalic Venous Cutdown for Implantation of Cardiac Electronic Devices

Clinical Trial Summary

Venous access is a fundamental step in lead insertion for endovenous cardiac implantable electronic devices (CIED). Cephalic vein cutdown is the most widely used technique in Europe. Ultrasound-guided axillary vein access is a promising alternative but there is a lack of clinical evidence supporting this technique. The purpose of this study is to compare the efficacy and safety of ultrasound-guided axillary vein access versus cephalic venous cutdown for implantation of endovenous CIED. Half of patients is implanted using an ultrasound-guided axillary vein puncture. The other half is implanted using a cephalic vein cutdown. After venous access is achieved, implantation procedure is identical in the two arms.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Implantable Cardioverter-defibrillator
  • Pacemaker
Clinical Trial Details
NCT number NCT04649788
Study type Interventional
Source Hospices Civils de Lyon
Contact
Status Completed
Phase N/A
Start date July 17, 2020
Completion date November 25, 2022
View Details
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