CompletedPhase 4NCT01367743

Study Comparing the Efficacy and Tolerability of Epinephrine and Norepinephrine in Cardiogenic Shock

Studying Cardiogenic shock

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Key facts

Sponsor
Central Hospital, Nancy, France
Principal Investigator
Philippe VIGNON, Dr
CHU Limoges
Intervention
epinephrine perfusion(drug)
Enrollment
58 enrolled
Eligibility
18 years · All sexes
Timeline
2011 – 2016

Study locations (11)

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 NCT01367743 on ClinicalTrials.gov

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