CompletedPhase 2NCT04325035
The Safety and Efficacy of Istaroxime for Pre-Cardiogenic Shock
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
- Windtree Therapeutics
- Principal Investigator
- Marco Metra, MDAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia, Italy
- Intervention
- Istaroxime(drug)
- Enrollment
- 90 enrolled
- Eligibility
- 18-85 years · All sexes
- Timeline
- 2020 – 2024
Study locations (13)
- Tufts Medical Center, Boston, Massachusetts, United States
- Hospital Italiano de Bueno Aires, Capital Federal, Buenos Aires, Argentina
- Santorio Guemes, Capital Federal, Buenos Aires, Argentina
- Hospital Privado de Rosario, Rosario, Sante Fe, Argentina
- Instituto Cardiovascular de Rosario, Rosario, Sante Fe, Argentina
- Santorio de la Trinidad Palermo, Buenos Aires, Argentina
- Azienda Ospedaliera Santi Antonio e Biagio e Cesare Arrigo, Alessandria, Italy
- UOC Cardiologia, ASST degli Spedali Civili di Brescia Pizzale Spedali Civili 1, Brescia, Italy
- IRCCS San Raffaele Scientific Institute, Milan, Italy
- Uniwersytecki Szpital Kliniczny, Centrum Chorub Serca, Wroclaw, Lower Silesian Voivodeship, Poland
- Uniwersytecki Szpital Kliniczny w Białymstoku, Bialystok, Poland
- Uniwersytecki Szpital Kliniczny w Opolu, Opole, Poland
- 4 Wojskowy Szpital Kliniczny, Wroclaw, Poland
Collaborators
Momentum Research, Inc.
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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