Registry Experience at the Washington Hospital Center With Drug Eluting Stents - Synergy

2016-07-06 23:08:21 | BioPortfolio


To compare the incidence of major adverse cardiac events among a series of patients receiving the Synergy drug-eluting stent with bioabsorbable polymer to historical controls who have received the Promus Premier drug-eluting stent with durable polymer.


The primary objective of this observational, real-world single-center registry is to compare the incidence of major adverse cardiac events among a series of patients receiving the Synergy drug-eluting stent with bioabsorbable polymer to historical controls who have received the Promus Premier drug-eluting stent with durable polymer. The investigators hypothesize that the long-term incidence (each year following implantation, up to 4 years) of major adverse cardiovascular events, after propensity matching for stent type, will be similar between Synergy and Xience V.

Study Design

Time Perspective: Retrospective


Incidence of Major Adverse Cardiac Events


PCI with Synergy Stent


MedStar Washington Hospital Center
District of Columbia
United States


Not yet recruiting


Medstar Research Institute

Results (where available)

View Results


Published on BioPortfolio: 2016-07-06T23:08:21-0400

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