WithdrawnPhase 2NCT00832728
Safety and Efficacy of the Extracorporeal Liver Assist Device (ELAD®) In Patients With Fulminant Hepatic Failure (FHF)
Studying Acute liver failure
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
- Vital Therapies, Inc.
- Principal Investigator
- Robert A AshleyVital Therapies, Inc.
- Intervention
- Standard of Care(other)
- Eligibility
- 10-65 years · All sexes
- Timeline
- 2009 – 2011
Study locations (12)
- Scripps Green Hospital, La Jolla, California, United States
- Cedars Sinai Medical Center, Los Angeles, California, United States
- California Pacific Medical Center, San Francisco, California, United States
- Loyola University Medical Center, Chicago, Illinois, United States
- University of Chicago Medical Center, Chicago, Illinois, United States
- Indiana University, Indianapolis, Indiana, United States
- Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana, United States
- New York University Medical Center, New York, New York, United States
- University of Rochester, Strong Memorial, Rochester, New York, United States
- Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
- Temple University Hospital, Philadelphia, Pennsylvania, United States
- University of Virginia, Charlottesville, Virginia, United States
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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