Status:
COMPLETED
Japan-Drug Eluting Stents Evaluation; a Randomized Trial
Lead Sponsor:
Associations for Establishment of Evidence in Interventions
Conditions:
Coronary Artery Disease
Eligibility:
All Genders
20+ years
Phase:
NA
Brief Summary
To evaluate the procedural, short and long term clinical outcomes of the TAXUS stent compared to Cypher stent in coronary arteries of ≥ 2.5 and ≤ 3.75 mm in the reference vessel diameter with a lesion...
Detailed Description
In these days, meta-analyses have been conducted in large scale and small scale studies, but there has been no conclusion yet stating which one of the stents, either Cypher stent or TAXUS stent, is su...
Eligibility Criteria
Inclusion
- Patient is ≥ 20 years old
- Patient suitable for percutaneous coronary intervention (PCI)
- Patient with signed informed consent
- Patient judged suitable to receive anti-platelet drugs (clopidogrel bisulfate or ticlopidine hydrochloride, etc.) in principle for at least 6 months after procedure, and ideally up to 12 months in patients who are not at high risk of bleeding, based on ACC/AHA guideline
- Patient with up to 3 lesions (with ≥ 50% of stenosis) in the maximum of 2 targeted vessels to be treated at once
- Patient with reference vessel diameter (RVD) of 2.5 mm to 3.75 mm by visual observation
- Patient with length of each lesion of up to 46 mm by visual assessment
- Patient eligible for implementation of drug eluting stent.
Exclusion
- Patient with any planned treatment in the targeted vessel with a drug eluting stent other than in this study
- Patient with acute myocardial infarction (AMI) (including non-ST segment elevation MI) developed within 7 days before the procedure
- Patient participating in a currently ongoing registry or clinical study, or receiving a treatment which may affect the endpoints of this study
- Patient of childbearing potential with a positive pregnancy test within 14 days before the procedure, or lactating
- Patient who has history of allergy against Sirolimus, Paclitaxel, polymers or stainless steel
- Patient who has history of side-effect against anti-platelet drugs or anti-coagulation drugs
- Patient with serious hepatic dysfunction
- Patient with left ventriculogram ejection fraction of 35% or less
- Patient with three target vessels in need of PCI treatment
- Patient with serious renal dysfunction (serum creatinine value 2mg/dL or higher)
- Patient currently receiving artificial dialysis
- Patient with a malignant tumor (cancer) diagnosed within 5 years before the procedure
- Patient who has received PCI treatment within the past one year
- Patient with chronic total occlusion (CTO) or TIMI flow 2 or less
- Patient with \>50% stenosis in left main coronary artery
- Patient with \>50% stenosis in side branch ostial for which stenting in the side branch lesion is required (KBT for side branch is accepted)
- Patient with in-stent restenosis in the target lesion implanted with a bare-metal or drug eluting stent
- Patient who has target lesion in saphenous vein graft
- Patient judged non-eligible by the physician in charge.
Key Trial Info
Start Date :
March 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
Estimated Enrollment :
3500 Patients enrolled
Trial Details
Trial ID
NCT00708669
Start Date
March 1 2008
Last Update
November 5 2014
Active Locations (122)
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1
Aichi Medical University Hospital
Aichi, Japan
2
Japan Labour Health and Welfare Organization, Kansai Rosai Hospital
Amagasaki, Japan
3
Asahikawa-Kosei General Hospital
Asahikawa, Japan
4
Sakakibara Memorial Hospital
Fuchū, Japan