Comparison of Strut Coverage With OPTIMAX Versus SYNERGY Stents

Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2015
The purpose of this study is to compare vascular healing of the stented segment after deployment of titanium-nitride-oxide coated cobalt-chromium OPTIMAX™ bio-active stent (BAS) and SYNERGY™ everolimus-eluting stent (EES) in patients with acute coronary syndromes requiring percutaneous coronary intervention. Patients treated with BAS will be treated with DAPT for at least 4 weeks after the procedure followed by aspirin alone, while patients in the EES group will be treated with DAPT, at least for 6 months post procedure. In addition, this study will collect initial information about the safety and effectiveness of the BAS in comparison with EES group at 30 days, 6 months, and 12 months.
Epistemonikos ID: edabe3619d7f99b84b935eee54ffaf77c3af9833
First added on: May 12, 2024