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A Study Evaluating ClariVein With a Sclerosing Agent for the Treatment of Venous Insufficiency — VICARES  

Venous Insufficiency Clinical Trial

Official title:
A Prospective, Randomized, Controlled, Multi-Center, Double Blind Study of ClariVein RES for Treatment of Venous Insufficiency Associated With Incompetent Saphenous Veins Due to Superficial Venous Reflux

Clinical Trial Summary

VICARES is a prospective randomized, controlled, multi-center, double blind study treating venous insufficiency associated with incompetent saphenous veins with 1% and 3% Sodium Tetradecyl Sulfate (STS) solution utilizing the ClariVein system.

Clinical Trial Description

Approximately 50 subjects diagnosed with an incompetent saphenous vein will be randomized to either 1% STS or 3% STS solution delivered by the ClariVein system under ultrasound guidance. Study duration for individual study patients, including follow-up visits, is anticipated to be approximately 16 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03311269
Study type Interventional
Source Vascular Insights, LLC
Contact
Status Terminated
Phase Phase 2
Start date September 22, 2017
Completion date March 27, 2020
View Details
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