The purpose of this study was to determine whether Sirolimus stent implantation is effective in reducing neointimal hyperplasia as compared to Bare metal stent in diabetic patients with de novo coronary artery stenosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
160
Drug eluting stent implantation
Hospital Clinico San carlos
Madrid, Madrid, Spain
The primary endpoint of this study was in-segment late lumen loss as assessed by quantitative coronary angiography
Time frame: 270-day follow-up
Other angiographic parameters of restenosis such as binary restenosis, and minimal luminal diameter; major adverse cardiac events including cardiac death, myocardial infarction, target lesion (in-segment zone) revascularization stent thrombosis
Time frame: 1, 9, 12 and 24-month follow-up
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