UnknownPhase 2NCT00004315
Phase II Pilot Study to Compare the Bioavailability of Buffered, Enteric-Coated Ursodiol With Unmodified Ursodiol for Chronic Cholestatic Liver Disease and Cystic Fibrosis-Associated Liver Disease
Studying Cystic fibrosis
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
- National Center for Research Resources (NCRR)
- Principal Investigator
- William Balistreri, M.DChildren's Hospital Medical Center, Cincinnati
- Intervention
- ursodiol(drug)
- Enrollment
- 20 enrolled
- Eligibility
- All sexes
- Timeline
- 1995
Study locations (1)
- Children's Hospital Medical Center - Cincinnati, Cincinnati, Ohio, United States
Collaborators
Children's Hospital Medical Center, Cincinnati
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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