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Clinical Trial Summary

The goal of this project is to provide an improvement in wire performance to expedite crossing difficult lesions in the coronary vasculature.


Clinical Trial Description

This Early Feasibility Study (EFS) is proposed to evaluate the initial safety and efficacy of the VasoStar guidewire system to cross complex coronary vascular lesions in non-tortuous arterial segments which are resistant to crossing with a traditional interventional guidewire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06193954
Study type Interventional
Source VasoStar, LLC
Contact Mihaela Plesa
Phone 440 266 8226
Email fvtinfo@frantzgroup.com
Status Not yet recruiting
Phase N/A
Start date June 13, 2024
Completion date May 31, 2025

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