A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral Stent System

NACompletedINTERVENTIONAL
Enrollment

104

Participants

Timeline

Start Date

May 31, 2007

Primary Completion Date

July 31, 2008

Study Completion Date

February 28, 2010

Conditions
AtherosclerosisPeripheral Vascular Disease
Interventions
DEVICE

Dynalink®-E everolimus-eluting peripheral stent

Stenting of atherosclerotic de novo or restenotic lesions (\> 50% stenosis) in the native superficial femoral or proximal popliteal artery

DEVICE

Dynalink®-E, everolimus-eluting peripheral stent

Stenting of atherosclerotic de novo or restenotic lesions (\> 50% stenosis) in the native superficial femoral or proximal popliteal artery

Trial Locations (10)

1090

Allgemeines Krankenhaus der Stadt Wien- AKH Wien, Vienna

3600

ZOL St. Jan, Ghent

9000

University Hospital, Ghent

9020

Landeskrankenhaus Klagenfurt, Klagenfurt

13347

The Jewish Hospital Berlin, Berlin

72076

University Hospital Tübingen, Tübingen

79189

Herzzentrum Bad Krozingen, Bad Krozingen

83013

Casa di Cura di Montevergine, Mercogliano

Unknown

Sint Blasius Hospital, Dendermonde

04289

Herzzentrum Leipzig, Leipzig

Sponsors
All Listed Sponsors
lead

Abbott Medical Devices

INDUSTRY