MedTrace Logo

Evaluation of Effectiveness and Safety of PROMUS Element Stent (IRIS-ELEMENT )

NCT01350791 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3001

Last updated 2017-07-21

No results posted yet for this study

Summary

This study is a non-randomized, prospective, open-label registry to compare the efficacy and safety of Promus Element stents versus first-generation drug-eluting stent (DES) in patients with coronary artery disease.

Conditions

Sponsors & Collaborators

  • CardioVascular Research Foundation, Korea

    collaborator OTHER

  • Boston Scientific Corporation

    collaborator INDUSTRY

  • Seung-Jung Park

    lead OTHER

Principal Investigators

  • Seung-Jung Park, MD, PhD · Asan Medical Center

  • Ki Bae Seung, MD, PhD · Seoul St. Mary's Hospital, Catholic University of Korea

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2013-10-31
Completion
2016-12-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

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 NCT01350791 on ClinicalTrials.gov