Coronary Artery Lesions clinical trials at UC Health
1 research study open to new patients
A Study of the Experimental XIENCE Device System for Patients Who Need Coronary Stenting (device to keep a heart artery open)
“The study will research the safety of aspirin plus 3 months of a second blood thinner in coronary stenting procedures.”
open to eligible people ages 18 years and up
XIENCE 90 study is a prospective, single arm, multi-center, open label trial to evaluate the safety of 3-month dual antiplatelet therapy (DAPT) in subjects at high risk of bleeding (HBR) undergoing percutaneous coronary intervention (PCI) with the approved XIENCE family of coronary drug-eluting stents. The XIENCE family stent systems include commercially approved XIENCE Xpedition Everolimus Eluting Coronary Stent System (EECSS), XIENCE Alpine EECSS, XIENCE PROX EECSS [rebrand of the XIENCE Xpedition Stent System and is only available outside of the United States (OUS)], XIENCE PROA EECSS (rebrand of the XIENCE Alpine Stent System and is only available OUS) and XIENCE Sierra EECSS of coronary drug-eluting stents.
at UC Davis