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Sponsored by: |
Rigshospitalet, Denmark |
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Information provided by: | Rigshospitalet, Denmark |
ClinicalTrials.gov Identifier: | NCT00151658 |
The purpose of this study is to evaluate the clinical and angiographic outcome of implantation of stents eluting or not eluting Sirolimus in patients with complex coronary artery lesions suitable for percutaneous coronary intervention.
Condition | Intervention |
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Ischaemic Heart Disease |
Device: Coronary Drug Eluting Stents for PCI |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Randomized Multicenter Comparison of Sirolimus Versus Bare Metal Stent Implantation in Complex Coronary Lesions. Acronym: Scand Stent |
Estimated Enrollment: | 322 |
Study Start Date: | October 2002 |
Estimated Study Completion Date: | June 2006 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Stable, or unstable angina and/or objective signs of myocardial ischaemia Lesions should be de novo and located in native vessels with a diameter > 2.25 mm.
Complex lesions to be included should have at least one of the following characteristics:
Exclusion Criteria:
Patients:
Lesions:
Study ID Numbers: | SCANDSTENT |
Study First Received: | September 8, 2005 |
Last Updated: | September 12, 2005 |
ClinicalTrials.gov Identifier: | NCT00151658 History of Changes |
Health Authority: | Denmark: National Board of Health |
Coronary complex lesions Restenosis Drug eluting stents |
Sirolimus Heart Diseases Myocardial Ischemia Vascular Diseases Ischemia |
Heart Diseases Myocardial Ischemia Vascular Diseases Cardiovascular Diseases |