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YUKON-drug-eluting Stent Below The Knee - Randomised Double-blind Study

NCT00664963 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2014-12-17

No results posted yet for this study

Summary

The purpose of this study is to compare the effectiveness of the treatment with balloon-expandable YUKON-BTX-Sirolimus-eluting stent over the treatment with YUKON-BTX uncoated stent in patients with ischemic infrapopliteal arterial disease.

Conditions

  • Arterial Occlusive Diseases

Interventions

DEVICE

Implantation of YUKON Sirolimus-eluting Stent

Implantation of YUKON Sirolimus-eluting Stent

DEVICE

Implantation of YUKON Stent (uncoated)

Implantation of YUKON Stent (uncoated)

Sponsors & Collaborators

  • Herz-Zentrums Bad Krozingen

    lead OTHER

Principal Investigators

  • Thomas Zeller, MD · Herz-Zentrum Bad Krozingen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-04-30
Primary Completion
2010-03-31
Completion
2010-04-30

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 NCT00664963 on ClinicalTrials.gov