Registry Experience at the Washington Hospital Center, DES - Xience V

Completed

Conditions studied: Coronary Artery Disease

In brief

Single center registry of patients who have received a Xience V everolimus-eluting stent at the Washington Hospital Center, with the primary objective to assess clinical success and safety at 30 days, 6 months and 1 year post-implantation.

Key facts

Study ID

NCT01003977

Run by

Rebecca Torguson

People needed

6069

Starts

2009-08-01

Expected to finish

2013-09-01

Last updated by the study team

2020-01-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients, male or female, >18 years of age
• Patients who received at least one Xience V drug-eluting stent at the Washington Hospital Center

You may not qualify if…

• Patients who received another type of DES (other than Xience V) or a bare metal stent at the time of initial Xience V stent implantation

Where it is running

• Washington Hospital Center — Washington D.C., District of Columbia, United States

Full record on ClinicalTrials.gov

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