UnknownPhase 4NCT03387605
Effect of Ivabradine in Stage D HF/Cardiogenic Shock Patients on Dobutamine
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
- Loyola University
- Principal Investigator
- Eugenia Raichlin, MDLoyola University
- Intervention
- Ivabradine(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 18-99 years · All sexes
- Timeline
- 2018 – 2020
Study locations (1)
- Loyola University Medical Center, Maywood, Illinois, United States
Collaborators
Amgen
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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