NCT03857906View on ClinicalTrials.gov

Evaluation of Prophylactic Use of a Preoperative IABP in High-Risk Coronary Artery Bypass Graft Surgery

CompletedOBSERVATIONAL

Enrollment

129

Participants

Timeline

Start Date

October 21, 2014

Primary Completion Date

February 21, 2018

Study Completion Date

January 19, 2019

Conditions

Ischemic CardiomyopathyHeart Failure

Interventions

DEVICE

Intra-Aortic Ballon Pump insertion

The IABP (Ultraflex IAB 7.5F, 2.5mm; Arrow International, Reading, PA) was inserted percutaneously through the right femoral artery in the previous 1 - 6 hours before the scheduled surgery. Positioning of the IABP was guided by radioscopy. The balloon size was based on the patient's height (30, 40 or 50 cc). Transesophageal echocardiography was used to confirm correct IABP placement before and after CABG

All Listed Sponsors

collaborator

Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado

OTHER_GOV

lead

"CMN 20 de Noviembre"

OTHER

NCT03857906 - Evaluation of Prophylactic Use of a Preoperative IABP in High-Risk Coronary Artery Bypass Graft Surgery | Biotech Hunter | Biotech Hunter