RecruitingPhase 3NCT05879276
Effect at 3 Months of Early Empagliflozin Initiation in Cardiogenic Shock Patients on Mortality, Rehospitalization, Left Ventricular Ejection Fraction and Renal Function.
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
- Central Hospital, Nancy, France
- Principal Investigator
- Nicolas GIRERD, MD PhDCHRU of NANCY
- Intervention
- Empagliflozin 10 MG(drug)
- Enrollment
- 164 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2027
Study locations (8)
- CHR Metz - Thionville, Ars-Laquenexy, France
- CHU de Besançon, Besançon, France
- CHU de Dijon Bourgogne, Dijon, France
- CHU Lille, Lille, France
- CHU Reims, Reims, France
- Hôpitaux Universitaires de Strasbourg, Strasbourg, France
- CHRU de NANCY - réanimation médicale, Vandœuvre-lès-Nancy, France
- Chru Nancy - Usic, Vandœuvre-lès-Nancy, 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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