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The purpose of this study is to evaluate the clinical safety and effectiveness of the Resolute Onyx stent in subjects deemed at high risk for bleeding and/or medically unsuitable for more than one-month DAPT treatment receiving reduced duration (one month) of DAPT following stent implantation.
View this clinical trail on ClinicalTrials.gov.
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For more information about a financial conflict of interest (FCOI), review the Essentia Health FCOI policy.
Last Updated: 12/06/2018