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

Withdrawn before enrolling

Conditions studied: Coronary Artery Disease

In brief

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.

Key facts

Study ID
NCT01003795
Run by
Medstar Health Research Institute
People needed
0
Starts
2009-10-01
Expected to finish
2013-10-01
Last updated by the study team
2020-10-19

Who can join

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

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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