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Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atherosclerosis

NCT03151018 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 4000

Last updated 2017-05-12

No results posted yet for this study

Summary

The objectives of this study are

1. To establish a prospective registry of the whole patients who received percutaneous coronary intervention with Resolute Onyx™ stent.
2. To evaluate the long-term efficacy and safety of coronary stenting with the Resolute Onyx™ stent.
3. To compare the long-term efficacy and safety of coronary stenting between the Resolute Onyx™ stent and other contemporary drug-eluting stents which had established their own registry.

Conditions

Interventions

DEVICE

Resolute Onyx

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Seoul National University Hospital

    lead OTHER

Principal Investigators

  • Hyo-soo Kim, MD, PhD · Seoul National University Hospital

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2018-05-31
Completion
2021-05-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03151018 on ClinicalTrials.gov