250
Participants
Start Date
July 10, 2025
Primary Completion Date
September 30, 2027
Study Completion Date
October 30, 2028
Impella
US commercially approved Impella CP is the device that study inclusion will be based on. Only patients with AMICS who receive Impella CP as the first Impella device after cardiogenic shock onset will be included in the study.
NOT_YET_RECRUITING
Ascension via Christi, Wichita
RECRUITING
New Mexico Heart, Albuquerque
RECRUITING
St. Joseph Hospital Orange, Orange
Lead Sponsor
Abiomed Inc.
INDUSTRY