Randomized comparison between bare-metal stent plus colchicine versus drug-eluting stent alone in prevention of clinical adverse events after percutaneous coronary intervention

Author:

Correa-Sadouet Camila1,Rodríguez-Granillo A Matías123,Gallardo Camila1,Mieres Juan23,Fontana Lucía1,Curotto María Valeria1,Wainer Pedro4,Allende N Gustavo5,Fernández-Pereira Carlos23,M Vetulli Héctor1,la Hoz R Pérez de6,Kastrati Adnan7,Rodríguez Alfredo E23,

Affiliation:

1. Cardiology Department, Sanatorio Otamendi, Ciudad de Buenos Aires, Argentina

2. Interventional Cardiology Department, Sanatorio Otamendi, Ciudad de Buenos Aires, Argentina

3. Centro de Estudios en Cardiología Intervencionista, Ciudad de Buenos Aires, Argentina

4. Internal Medicine Department, Sanatorio Otamendi, Ciudad de Buenos Aires, Argentina

5. Cardiology Department, Clínica IMA, Adrogué, Provincia de Buenos Aires, Argentina

6. Cardiology Department, Hospital de Clínicas José de San Martín, Ciudad de Buenos Aires, Argentina

7. Deutsches Herzzentrum Munich, Germany

Abstract

The use of colchicine is associated with a significant reduction of cardiac adverse events in patients with coronary artery disease. Past small randomized trials with oral immunosuppressive or anti-inflammatory therapies have demonstrated a reduction of adverse clinical events after bare metal stent implantation. The potential role of adjunctive colchicine after bare-metal stent implantation, compared with drug-eluting stent alone, is unknown. The primary end point of the study will be to compare cost–effectiveness at 1 year of follow-up of coronary intervention with bare-metal stent implantation plus 1 mg of colchicine during 3 months versus percutaneous coronary intervention with drug-eluting stent implantation alone. ClinicalTrials.gov  identifier: NCT04382443

Publisher

Future Medicine Ltd

Subject

Cardiology and Cardiovascular Medicine,Molecular Medicine

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