CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulmonary Bypass

NACompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

October 31, 2008

Primary Completion Date

May 31, 2013

Study Completion Date

September 30, 2013

Conditions
Heart Failure
Interventions
DEVICE

CentriMag Ventricular Assist System

All eligible subjects will receive the CentriMag Ventricular Assist System. The system is comprised of a single-use centrifugal blood pump, a motor, a primary drive console, a back up drive console and cannulae. Blood from the failing heart is directed from the ventricle or the atrium to the inlet of the pump via an inlet cannula. Blood exits through the outlet port of the pump through the outlet cannula ultimately to the pulmonary or systemic circulation. The system can be used in either a right, left or biventricular configuration.

Trial Locations (14)

10032

New York Columbia Presbyterian Hospital, New York

14642

University of Rochester, Rochester

15213

University of Pittsburgh Medical Center, Pittsburgh

19104

Hospital of the University of Pennsylvania, Philadelphia

21201

University of Maryland, Baltimore

27710

Duke University Medical Center, Durham

40536

University of Kentucky, Lexington

53215

St. Luke's Medical Center, Milwaukee

55455

Fairview University Medical Center, Minneapolis

77030

St. Luke's Episcopal, Houston

84107

Intermountain Medical Center, Murray

84132

University of Utah, Salt Lake City

85054

Mayo Clinic Hospital, Arizona, Phoenix

06510

Yale University, New Haven

Sponsors
All Listed Sponsors
collaborator

Thoratec Corporation

INDUSTRY

lead

Abbott Medical Devices

INDUSTRY