RecruitingNot applicableNCT05366452

Evaluation of the Efficacy of Early Implantation of a Percutaneous Left Ventricular Assist Devices in Acute Coronary Syndrome Complicated by Cardiogenic Shock Compared to Conventional Therapy: a Prospective, Multicenter, Randomized, Controlled and Open-label Clinical Trial

Studying Cardiogenic shock

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Key facts

Sponsor
Assistance Publique Hopitaux De Marseille
Principal Investigator
François CREMIEUX
Assistance Publique Hopitaux De Marseille
Intervention
IMPELLA CP(device)
Enrollment
204 enrolled
Eligibility
18-80 years · All sexes
Timeline
20222026

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05366452 on ClinicalTrials.gov

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