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Multicenter Postmarket Surveillance Registry Evaluating Performance and Long Term Safety of the Presillion Stent

NCT00968019 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 318

Last updated 2013-03-13

Study results available
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Summary

The purpose of this study is: To evaluate the safety and performance of the Presillion stent in routine clinical practice.

Conditions

  • Coronary Arteriosclerosis

Interventions

DEVICE

Presillion stent

Centers will use commercially available Presillion Stents as recommended according to the Instruction For Use (IFU).

Sponsors & Collaborators

  • Johnson and Johnson, S.A.

    lead INDUSTRY

Principal Investigators

  • Angel Cequier, MD, PhD · Hospital Universitario de Bellvitge

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2011-04-30
Completion
2011-05-31

Countries

  • Portugal
  • Spain

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 NCT00968019 on ClinicalTrials.gov