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Clinical Trial Summary

To compare the MT005 (MiStent) with the XIENCE with respect to target lesion failure (TLF) at 12 months in a non-inferiority trial in a "real world" patient population and to confirm that the domestic extrapolation of the DESSOLVE III study results is valid.


Clinical Trial Description

This is a prospective, randomized, 1:1 balanced, controlled, double-blind, multi-center study comparing clinical outcomes at 12 months between MT005 (MiStent) and XIENCE in an all-comers population, including patients with symptomatic coronary artery disease including patients with chronic stable angina, silent ischemia, and acute coronary syndromes, who qualify for percutaneous coronary interventions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02972671
Study type Interventional
Source Micell Technologies
Contact
Status Active, not recruiting
Phase N/A
Start date November 28, 2016
Completion date April 30, 2022

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