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Varithena Versus Endothermal Ablation of the Great Saphenous Vein (VERITAS) — VERITAS  

Varicose Veins Clinical Trial

Official title:
A Phase 4 Randomized Trial Comparing Varithena to Endothermal Ablation for the Treatment of the Great Saphenous Vein

Clinical Trial Summary

The purpose of this study is to observe insights into the benefits of Varithena compared to Endothermal Ablation (ETA) in the treatment of the great saphenous vein.

Clinical Trial Description

To collect comparative evidence on patient reported outcomes of Varithena compared to ETA when used to treat the incompetent great saphenous vein (GSV). ETA will include either radiofrequency ablation or endovenous laser ablation according to the site's standard practice. To provide long term (1-year, 2-year, and 3-year) outcomes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05312970
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Terminated
Phase Phase 4
Start date February 10, 2023
Completion date April 4, 2024
View Details
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