Acute Coronary Syndrome Clinical Trial
Official title:
Prospective Multicenter Observational Study for Evaluating Efficacy and Safety of Short Duration of Dual Antiplatelet Therapy After Genoss DES Sirolimus-eluting Stent Implantation in Patients With Coronary Artery Disease
The investigators aimed to evaluate the safety and effectiveness of short-term DAPT (3 months for SCAD, 6 months for ACS) after PCI with Genoss DES in patients with coronary artery disease.
This study is a sponsor-initiated clinical trial (SIT) that enrolls patients with coronary artery disease who have undergone percutaneous coronary intervention using the GENOSS DES stent as research subjects, collects data on the patients' clinical and surgical procedures, and reports on clinical events. The investigators will track the outbreak. This study is a prospective, multicenter registration observational study that will enroll patients with coronary artery disease who underwent percutaneous coronary intervention with GENOSS DES at a total of five institutions. This study is a registered observation study and does not separately calculate the number of subjects, but plans to recruit a total of 1,000 subjects during the study period. ;
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