Coronary Artery Disease Clinical Trial
Official title:
Optimal Duration of Dual Antiplatelet Therapy After Drug Eluting Stent (DES) Implantation
To compare treatment with aspirin alone versus the combined antiplatelet treatment aspirin and clopidogrel after 12 months of combined antiplatelet treatment following drug-eluting stent (DES) implantation.
Drug-eluting stents (DES) substantially reduce restenosis compared with bare metal stents
and represent a significant advance in percutaneous coronary interventions (PCIs).
Accordingly, DES have been rapidly adopted into practice and are currently used in the
majority of PCI procedures. Despite their rapid acceptance, DES are not without limitations.
In particular, patients who receive DES (like those who receive conventional bare metal
stents) remain at risk of a 1% to 2% incidence of stent thrombosis, which is often
associated with devastating consequences like death or myocardial infarction. Understanding
and eliminating mediators of stent thrombosis are thus important goals for optimizing the
clinical benefits of DES. Delayed endothelial coverage after DES implantation has been
demonstrated and is thought to prolong the window of vulnerability to stent thrombosis.
Consequently, current recommendations for DES are: dual antiplatelet therapy for at least 12
months in patients at low risk of bleeding, especially with " off-label " use. Because of
rare but severe very late stent thrombosis, the dual antiplatelet therapy is more and more
prescribed in clinical practice for several years.But it has been clearly demonstrated that
the combination of aspirin and clopidogrel (the thienopyridine the most used) significantly
increase the rate of severe and moderate bleedings when compared to aspirin alone. This is
important if we consider the possibility or the necessity to prolong the combined
antiplatelet therapy after stent implantation.ProposalTo compare treatment with aspirin
alone versus the combined antiplatelet treatment with aspirin and clopidogrel after 12
months of combined antiplatelet treatment after DES implantation
NB : On the decision of the sponsor, the latest patient monitoring was advanced to September
30, 2014 instead of January 2015.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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