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Active Not RecruitingNCT02593994

IRIS-Onyx Cohort in the IRIS-DES Registry

Evaluation of Effectiveness and Safety of Resolute Onyx™ and Onyx Frontier™ in Routine Clinical Practice; A Multicenter, Prospective Observational Study

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
4,500 (actual)
Sponsor
Seung-Jung Park · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the relative effectiveness and safety of Onyx stent compared to other (drug eluting stents) DES.

Conditions

Interventions

TypeNameDescription
DEVICEOnyx Drug Eluting Stent group

Timeline

Start date
2015-10-01
Primary completion
2026-12-31
Completion
2030-12-31
First posted
2015-11-02
Last updated
2026-01-15

Locations

31 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02593994. Inclusion in this directory is not an endorsement.

IRIS-Onyx Cohort in the IRIS-DES Registry (NCT02593994) · Clinical Trials Directory