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Genoss DES in Patients With a High Risk of Ischemic Events (GENTLE Registry)

Coronary Artery Disease Clinical Trial

Official title:
Safety and Efficacy of Sirolimus-eluting Biodegradable Abluminal Coating Stents in Patients With a High Risk of Ischemic Events: a Single-center, Prospective, Observational Trial (GENTLE Registry)

Clinical Trial Summary

This is a prospective cohort study to evaluate the long-term effect and safety of Genoss drug-eluting stents (DES) in patients with coronary artery disease with high ischemic features.

Clinical Trial Description

It is known that ischemic events after percutaneous coronary intervention (PCI) or coronary artery bypass surgery (CABG) increase as the anatomical, physiological, or functional complexity of coronary artery disease increases. Recently, the concept of complex higher-risk and clinically indented procedure (CHIP) has been proposed, which includes patients with various medical conditions, patients with various heart conditions, and patients with technically complex PCI. Until now, Genoss stents have no data on the evaluation of stents in patients with coronary artery disease and high ischemic features. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05448625
Study type Observational [Patient Registry]
Source Yonsei University
Contact Yongcheol Kim, MD, Phd
Phone +82-031-5189-8967
Email yongcheol@yuhs.ac
Status Recruiting
Phase
Start date May 26, 2022
Completion date December 31, 2026
View Details
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