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Comparison of Cypher Select and Taxus Express Coronary Stents
This study has been completed.
Sponsors and Collaborators: Skejby Hospital
University of Aarhus
University of Copenhagen
Odense University Hospital
Information provided by: Skejby Hospital
ClinicalTrials.gov Identifier: NCT00388934
  Purpose

Randomized nine months clinical comparison of implantation of Taxol eluting (Taxus Express) and Sirolimus eluting (Cypher Select) stents in non-selected patients with coronary artery disease.


Condition Intervention Phase
Coronary Artery Disease
Angina Pectoris
Procedure: Percutaneous coronary intervention (PCI)
Phase IV

MedlinePlus related topics: Angina Coronary Artery Disease
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Safety Study
Official Title: Randomized Clinical Comparison of Cypher Select and Taxus Express Stent Implantation in Unselected Patients With Coronary Artery Disease.

Further study details as provided by Skejby Hospital:

Primary Outcome Measures:
  • MACE (cardiac death, MI, TVR, TLR, TVF)during 9 months

Secondary Outcome Measures:
  • Total death after 9 months, 2 and 3 years
  • Cardiac death after 9 months, 2 and 3 years
  • MI after 9 months, 2 and 3 years
  • TVL, TVR, TVF after 9 months, 2 and 3 years
  • Stent thrombosis after 9 months, 2 and 3 years

Estimated Enrollment: 2000
Study Start Date: August 2004
Estimated Study Completion Date: January 2009
Detailed Description:

Design:

  • Randomized open multicentre trial.

Patients:

  • 1800 patients with coronary artery disease scheduled for percutaneous coronary intervention with stent implantation.

Inclusion criteria:

  • Patients with coronary artery disease scheduled for percutaneous coronary intervention with stent implantation.
  • Signed informed conscent.

Exclusion critteria:

  • Participation in other stent studies.

Randomization:

  • Implantation of Taxus Express og Cypher Select stents.

Primary end-point:

  • Combined end-point of cardiac death, new revascularization (PCI or CABG) or myocardial infarction after nine months.

Secondary end-påoints:

  • Total death after nine months
  • Cardiac death after nine months
  • Myocardial infarction after nine months
  • Index vessel myocardial infarction after nine months
  • Target lesion revascularization
  • Target vessel revascularization
  • Stent thrombosis after nine months

End-point evaluation:

  • End-points will be ajudicated by an independent end-point committee
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Planned implantation of drug eluting stent
  • Written informed consent

Exclusion Criteria:

  • Planned intervention with other stents than study stents
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00388934

Sponsors and Collaborators
Skejby Hospital
University of Aarhus
University of Copenhagen
Odense University Hospital
Investigators
Principal Investigator: Anders Galloe, MD Gentofte Hospital, Copenhagen
  More Information

Publications indexed to this study:
Study ID Numbers: SORT-OUT II
Study First Received: October 16, 2006
Last Updated: May 8, 2007
ClinicalTrials.gov Identifier: NCT00388934  
Health Authority: Denmark: National Board of Health

Keywords provided by Skejby Hospital:
Percutaneous coronary intervention
Angina pectoris
Stent

Study placed in the following topic categories:
Arterial Occlusive Diseases
Coronary Disease
Signs and Symptoms
Heart Diseases
Myocardial Ischemia
Vascular Diseases
Angina Pectoris
Pain
Arteriosclerosis
Ischemia
Coronary Artery Disease
Chest Pain

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009