Active, not recruitingPhase 2NCT03799874
Safety and Efficacy Study of Inhaled Carbon Monoxide to Treat Acute Respiratory Distress Syndrome (ARDS)
Studying Adult acute respiratory distress syndrome
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
- Brigham and Women's Hospital
- Principal Investigator
- Rebecca Baron, MD, M.DBrigham and Women's Hospital
- Intervention
- Inhaled Carbon Monoxide at 200 ppm(drug)
- Enrollment
- 32 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2026
Study locations (7)
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Brigham and Women's Hospital, Boston, Massachusetts, United States
- Washington University, St Louis, Missouri, United States
- New York-Presbyterian Brooklyn Methodist Hospital, Brooklyn, New York, United States
- Weill Cornell Medical College, New York, New York, United States
- Duke Regional Hospital, Durham, North Carolina, United States
- Duke University Hospital, Durham, North Carolina, United States
Collaborators
Massachusetts General Hospital · Weill Medical College of Cornell University · Duke University · Durham VA Medical Center · New York Presbyterian Brooklyn Methodist Hospital · Duke Regional Hospital · U.S. Army Medical Research Acquisition Activity · Washington University School of Medicine
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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