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
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Assistance Publique Hopitaux De Marseille
- Principal Investigator
- François CREMIEUXAssistance Publique Hopitaux De Marseille
- Intervention
- IMPELLA CP(device)
- Enrollment
- 204 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2022 – 2026
Study locations (1)
- Assistance Publique Hopitaux de Marseille, Marseille, Bouche DU Rhone, France
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.
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