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

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

Summary

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.

Description

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

Conditions

Incidence of Major Adverse Cardiac Events

Intervention

PCI with Synergy Stent

Location

MedStar Washington Hospital Center
Washington
District of Columbia
United States

Status

Not yet recruiting

Source

Medstar Research Institute

Results (where available)

View Results

Links

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

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