Clinical Effects of Intra-aortic Balloon Support in Early Acute Coronary Syndrome and Non-Acute Coronary Syndrome Related Cardiogenic Shock

NANot yet recruitingINTERVENTIONAL
Enrollment

400

Participants

Timeline

Start Date

June 1, 2024

Primary Completion Date

June 1, 2027

Study Completion Date

June 1, 2027

Conditions
Cardiogenic Shock
Interventions
DEVICE

Intra-Aortic Balloon Pump

Patients who are randomized to the IABP-arm will be supported with IABP according to local, clinical guidelines (including algorithms for anticoagulation, verification of correct positioning and weaning strategies). The IABP console and disposables should be used according to the instructions for use, including the use of an appropriate-sized IABP balloon alligned with patient length and height.

Trial Locations (1)

3000 CA

Erasmus University Medical Center, Rotterdam

Sponsors
All Listed Sponsors
collaborator

Arrow International LCC (Subsidiary of Teleflex Inc.)

UNKNOWN

lead

Erasmus Medical Center

OTHER