Comparative Registry of the PROmus™, ENdeavor™ and CYpher™ Drug Eluting Stents

NCT00930878 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1934

Last updated 2017-02-03

No results posted yet for this study

Summary

The purpose of this study is to collect real-life data of the Promus™ stent, the Cypher™ stent and the Endeavor™ stent in routine clinical practice, and compare outcomes.

Conditions

  • Percutaneous Coronary Intervention

Interventions

DEVICE

Cardiac Stenting

Drug Eluting stent

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Christian Hamm, MD · Kerckhoff-Klinik GmbH

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-02-29
Primary Completion
2010-03-31
Completion
2010-03-31

Countries

  • Germany

Study Locations

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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 NCT00930878 on ClinicalTrials.gov