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Prospective Registry of Patients With Acute Coronary Syndrome Treated With GENOSS Stent — GENOSSACS  

Acute Coronary Syndrome Clinical Trial

Official title:
A Multi-center Prospective Registry of Patients With Acute Coronary Syndrome (ACS) Treated With GENOSSTM Sirolimus-eluting Stent

Clinical Trial Summary

The investigators intend to establish a multi-center prospective observational study to evaluate the effectiveness and safety of Genoss DES by registering and tracking patients treated for acute coronary syndrome (ACS) as research subjects using Genoss DES, which was manufactured purely with domestic technology.

Clinical Trial Description

This study is a sponsor-initiated clinical trial (SIT) that will enroll patients treated for acute coronary syndrome using the GENOSS stent as research subjects, collect data on the patients' clinical and surgical procedures, and track the occurrence of clinical events. . This study is a prospective, multicenter registration observational study enrolling patients with acute coronary artery disease treated using the GENOSS stent at a total of 10 institutions. Since this study is a registered observation study, the number of subjects is not calculated separately, but a total of 1,000 subjects are scheduled to be recruited during the study registration period. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06075368
Study type Observational [Patient Registry]
Source Genoss Co., Ltd.
Contact InHo Chae
Phone 010-9700-1676
Email ihchae@snu.ac.kr
Status Recruiting
Phase
Start date February 17, 2020
Completion date December 31, 2025
View Details
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