Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial

NACompletedINTERVENTIONAL
Enrollment

192

Participants

Timeline

Start Date

April 13, 2010

Primary Completion Date

March 9, 2012

Study Completion Date

September 5, 2012

Conditions
Abdominal Aortic Aneurysm
Interventions
DEVICE

PEVAR (ProGlide closure)

Percutaneous EVAR facilitated by the ProGlide closure device

DEVICE

SEVAR (IntuiTrak)

Standard vascular exposure for access prior to EVAR

DEVICE

PEVAR (Prostar XL closure)

Percutaneous EVAR facilitated by the Prostar XL closure device

Trial Locations (20)

22042

Inova Fairfax, Falls Church

22903

University of Virginia, Charlottesville

28801

Mission Hospital, Asheville

32608

VA Gainesville, Gainesville

33125

VA Miami, Miami

33176

Baptist Cardiac and Vascular Institute, Miami

33308

Holy Cross Medical Center, Fort Lauderdale

39401

Forrest General Hospital, Hattiesburg

44094

Lake Health, Willoughby

44195

Cleveland Clinic, Cleveland

53792

University of Wisconsin, Madison

57108

North Central Heart Hospital, Sioux Falls

60611

Northwestern University, Chicago

60616

Mercy Hospital, Chicago

75216

Dallas VA Medical Center, Dallas

77030

St. Luke's Hospital at Texas Heart Institute, Houston

92161

VA San Diego, San Diego

92357

Loma Linda VA Medical Center, Loma Linda

93120

Oklahoma Heart Hospital, Oklahoma City

03756

Dartmouth-Hitchcock Medical Center, Lebanon

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Abbott Medical Devices

INDUSTRY

lead

Endologix

INDUSTRY