RecruitingNCT06177743

IRIS-Coroflex NEO Cohort

Evaluation of Effectiveness and Safety of Coroflex ISAR NEO Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study


Sponsor

Seung-Jung Park

Enrollment

1,000 participants

Start Date

Jan 9, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The objective of this study is to evaluate the effectiveness and safety of Coroflex ISAR NEO stents in comparison to other drug-eluting stents (DES) in real-world practice.


Eligibility

Min Age: 19 Years

Inclusion Criteria3

  • Patients ≥ 19 years old
  • Patients receiving Coroflex ISAR NEO stents.
  • The patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethics Committee of the respective clinical site.

Exclusion Criteria3

  • Patients with a mixture of other DESs
  • Terminal illness with life expectancy <1 year.
  • Patients with cardiogenic shock

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICECoroflex ISAR NEO stent

Percutaneous coronary intervention with Coroflex ISAR NEO stent


Locations(11)

Asan Medical Center

Seoul, Songpa-gu, South Korea

Bucheon Sejong Hospital

Bucheon-si, South Korea

The Catholic Univ. of Korea BUCHEON ST.Mary's hospital

Bucheon-si, South Korea

Veterans Hospital

Daegu, South Korea

Chonnam National University Hospital

Gwangju, South Korea

Inje University Ilsan Paik Hospital

Ilsan, South Korea

Myongji Hospital

Ilsan, South Korea

Sejong Chungnam National University Hospital

Sejong, South Korea

Seoul National University Boramae Medical Center

Seoul, South Korea

The Catholic university of Korea, ST. Vincent's Hospital

Suwon, South Korea

Uijeongbu Eulji Medical Center

Uijeongbu-si, South Korea

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06177743


Related Trials