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A Study to Evaluate the Impact of Pre-procedural Intracoronary Nicorandil Injection to PRE

The aim of this study was to determine the effect of intra-coronary administration of nicorandil on the prevention of lowering of coronary blood flow for high-risk plaque lesions defined as the high value of lipid core burden index in patients with coronary artery disease who require stent treatment.

Condition(s)No-Reflow Phenomenon, Coronary Artery Disease, Percutaneous Coronary Intervention
StatusRecruiting
PhasePhase 4
Study typeInterventional
SummaryThe aim of this study was to determine the effect of intra-coronary administration of nicorandil on the prevention of lowering of coronary blood flow for high-risk plaque lesions defined as the high value of lipid core burden index in patients with coronary artery disease who require stent treatment.
Who can participateInclusion Criteria: 1. Over 19 years old 2. Patients who agree to the study plan and clinical follow-up plan, voluntarily decide to participate in this study, and consent in writing to the consent to use information 3. Patients who underwent NIRS-IVUS guided coronary stent surgery for coronary artery disease Exclusion Criteria: 1. Patients with TIMI ≤ 2 before coronary intervention 2. Subjects with known hypersensitivity or contraindications to the following drugs or substances: heparin, aspirin, clopidogrel, ticagrelor, prasugrel, rosuvastatin, ezetimibe, evolocumab, lansoprazole, cobalt chromium, stainless steel nickel And contrast agents (however, even a subject who is hypersensitive to contrast agents can register if they can be controlled by steroids and pheniramine, except for known
Ages19 Years
SexAll
Lead sponsorKorea University Anam Hospital
LocationsSeoul, South Korea
Start date2022-12-14
NCT IDNCT05427786
Official listinghttps://clinicaltrials.gov/study/NCT05427786

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