Dataset Information
A first-in-man study of sirolimus-eluting, biodegradable polymer coated cobalt chromium stent in real life patients.
Ontology highlight
ABSTRACT: Introduction
Despite considerable benefits associated with current drug-eluting stents, continued attention to the safety, efficacy, and deliverability of available drug-eluting stent has led to the development of newer stent.Methods
This study was a single-centre, prospective, non-randomized, first-in-man study which included clinical follow-up data was collected at 1, 8 and 12 months after the procedure. The study included 105 patients with de novo native coronary artery lesions including multi-vessel disease treated with Supralimus-Core® stent. Repeat angiography was performed 8 months post-stent implantation.Results
At quantitative coronary angiography 8-month luminal late loss was 0.39 ± 0.33 mm in-stent and 0.33 ± 0.35 mm in-segment. The incidence of any major adverse cardiac event at 30 days, 8 months and 12 months was 1 (1%), 6 (6%) and 7 (7%) respectively.Conclusion
This study demonstrates that the Supralimus-Core® SES is a safe and effective treatment for patients with obstructive coronary artery disease. ClinicalTrials.gov ID: NCT00811616.
SUBMITTER: Seth A
PROVIDER: S-EPMC3861257 | biostudies-literature | 2012 Nov-Dec
REPOSITORIES: biostudies-literature
Publications
A first-in-man study of sirolimus-eluting, biodegradable polymer coated cobalt chromium stent in real life patients.
Indian heart journal 20120727 6
<h4>Introduction</h4>Despite considerable benefits associated with current drug-eluting stents, continued attention to the safety, efficacy, and deliverability of available drug-eluting stent has led to the development of newer stent.<h4>Methods</h4>This study was a single-centre, prospective, non-randomized, first-in-man study which included clinical follow-up data was collected at 1, 8 and 12 months after the procedure. The study included 105 patients with de novo native coronary artery lesion ...[more]