IRIS-BVS AMI Registry

NCT02699671 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 69

Last updated 2021-09-13

No results posted yet for this study

Summary

The purpose of this study is to evaluate the relative effectiveness and safety of Bioresorbable Vascular Scaffold in acute myocardial infarction compared to other (drug eluting stents) DES.

Conditions

Interventions

DEVICE

Bioresorbable Vascular Scaffold

Sponsors & Collaborators

  • CardioVascular Research Foundation, Korea

    collaborator OTHER
  • Duk-Woo Park, MD

    lead OTHER

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2017-12-31
Completion
2017-12-31

Countries

  • South Korea

Study Locations

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Entities

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 NCT02699671 on ClinicalTrials.gov