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Long Term Safety Profile of the PRO-Kinetic ENERGY Coronary Stent System in Daily Clinical Practice

NCT01056120 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1026

Last updated 2016-02-01

No results posted yet for this study

Summary

To evaluate the clinical performance of the PRO-Kinetic ENERGY® coronary bare metal stent system in a patient population within that defined in the Instructions for Use.

Conditions

  • De Novo and Re-stenosed Coronary Artery Lesions

Interventions

DEVICE

Pro Kinetic Energy bare metal stent

PCI

Sponsors & Collaborators

  • Biotronik AG

    lead INDUSTRY

Principal Investigators

  • Raimund Erbel, MD · Klinik für Kardiologie Westdeutsches Herzzentrum Essen, Universitätsklinikum Essen, Hufelandstrasse 55, D-45122 Essen, Germany

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2013-02-28
Completion
2013-12-31

Countries

  • Austria
  • Belgium
  • France
  • Germany
  • Ireland
  • Israel
  • Latvia
  • Netherlands
  • Spain
  • Switzerland

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 NCT01056120 on ClinicalTrials.gov