CompletedNCT01568554
Clinical Diagnosis of Acute Porphyria
Studying Hereditary coproporphyria
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
- University of California, San Francisco
- Principal Investigator
- Bruce Wang, M.D.University of California at San Francisco
- Enrollment
- 148 enrolled
- Eligibility
- 15 years · All sexes
- Timeline
- 2011 – 2018
Study locations (6)
- UAB Porphyria Center, University of Alabama at Birmingham, Birmingham, Alabama, United States
- UCSF Porphyria Center, University of California at San Francisco, San Francisco, California, United States
- Mount Sinai Porphyria Comprehensive Diagnostic & Treatment Center, Mount Sinai School of Medicine, New York, New York, United States
- Wake Forest University School of Medicine, Winston-Salem, North Carolina, United States
- UTMB Porphyria Center, University of Texas Medical Branch, Galveston, Texas, United States
- Porphyria Center, University of Utah, Salt Lake City, Utah, United States
Collaborators
University of Texas · University of Alabama at Birmingham · Icahn School of Medicine at Mount Sinai · University of Utah · Carolinas Medical Center · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · Rare Diseases Clinical Research Network
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.
Open NCT01568554 on ClinicalTrials.gov