NCT00878527View on ClinicalTrials.gov

Safety and Performance Evaluation of CircuLite Synergy

NACompletedINTERVENTIONAL
Enrollment

63

Participants

Timeline

Start Date

June 29, 2007

Primary Completion Date

January 29, 2018

Study Completion Date

January 29, 2018

Conditions
Heart Failure
Interventions
DEVICE

CircuLite Synergy Pocket Circulatory Assist Device

Goal of successful implantation and follow-up for at least three months

Trial Locations (11)

3000

UZ Leuven, Leuven

10179

German Heart Centre Berlin, Berlin

20089

Humanitas Clinical and Research Center, Milan

30625

Hannover Medical School, Hanover

Medical School Hannover, Hanover

48149

University Hospital Muenster, Münster

50937

Heart Center Cologne University Hospital, Cologne

79106

University Hospital Freiburg, Freiburg im Breisgau

83348

National Institute of Cardiovascular Diseases Bratislava, Bratislava

04289

Heart Centre University Leipzig, Leipzig

UB9 6JH

Harefield Hospital, Harefield

All Listed Sponsors
lead

Medtronic Cardiac Rhythm and Heart Failure

INDUSTRY

NCT00878527 - Safety and Performance Evaluation of CircuLite Synergy | Biotech Hunter | Biotech Hunter