CompletedNCT00589225
Primary Hyperoxaluria Mutation Genotyping
Studying Primary hyperoxaluria
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
- Mayo Clinic
- Principal Investigator
- Dawn Milliner, MD, M.DMayo Clinic
- Intervention
- Genetic Analysis(genetic)
- Enrollment
- 902 enrolled
- Eligibility
- All sexes
- Timeline
- 2003 – 2014
Study locations (1)
- Mayo Clinic, Rochester, Minnesota, United States
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · Oxalosis and Hyperoxaluria Foundation (OHF)
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 NCT00589225 on ClinicalTrials.govOther trials for Primary hyperoxaluria
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