Promus - Registry Experience at the Washington Hospital Center, Drug-eluting Stent (DES)



Status:Completed
Conditions:Peripheral Vascular Disease, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:Any
Updated:2/4/2013
Start Date:October 2009
End Date:October 2012
Contact:Rebecca Torguson
Email:rebecca.torguson@medstar.net
Phone:202-877-2194

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P-REWARDS (Promus - Registry Experience at the Washington Hospital Center, DES)


Single-center registry of patients treated with at least one Promus, everolimus-eluting,
Stent, with the primary objective to assess clinical success and safety at 30 days, 6 months
and 1 year post-implantation.


Interventional cardiology was revolutionized by the invention of stents, initially with the
bare-metal stents (BMS) and recently with the drug-eluting stents (DES). The everolimus
eluting stents have shown very promising results in randomized clinical trials,
demonstrating a reduction of clinical and angiographic restenosis in comparison to BMS, and
comparable clinically-driven target lesion revascularization rates in comparison with
sirolimus-eluting stents. While registry data is available from outside of the United
States, it will be important to collect "real-world" data regarding the stent usage and
outcomes in the United States. In this study we propose to follow patients who received at
least one Promus® Stent for at least 1 year post initial stent implantation.

Inclusion Criteria:

- Patients, male or female, >18 years of age

- Patients who received at least one Promus drug-eluting stent at the Washington
Hospital Center

Exclusion Criteria:

- N/A
We found this trial at
1
site
110 Irving St NW
Washington, District of Columbia 20010
(202) 877-7000
Washington Hosp Ctr MedStar Washington Hospital Center is a not-for-profit, 926-bed, major teaching and research...
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from
Washington,
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