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DaVinci Registry(Distinctly Assess Vision in Coronary Intervention)

NCT00243438 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1300

Last updated 2009-01-28

No results posted yet for this study

Summary

Prospective Internet-Registry, Postmarketing-Surveillance, Registration and Follow-up of patients after Multi-Link VISION™ - Stent Implantation

Conditions

  • Coronary Disease

Interventions

DEVICE

Multilink Vision™ Stent (CE-labeled)

Patients who have diabetes and/or complex lesions and who have had a Multilink Vision™ Stent placed.

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Christian Hamm, MD · Kerckhoff-Klinik/ Benekestr. 2-8/ 61231 Bad Nauheim

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-07-31
Primary Completion
2005-03-31
Completion
2005-03-31

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 NCT00243438 on ClinicalTrials.gov