Primary Hyperoxaluria Mutation Genotyping/Phenotyping
NCT02340689 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1235
Last updated 2019-08-19
Summary
Specific mutations relating to hyperoxaluria will be determined via DNA analysis by the Mayo RKSC research staff.
Conditions
- Primary Hyperoxaluria
Interventions
- OTHER
-
Genetic Analysis
We will draw one tube of blood from your arm to obtain white blood cells. These white blood cells will be used as a source of DNA for genetic analysis.
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Dawn Milliner, MD · Mayo Clinic
Eligibility
- Min Age
- 1 Day
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-10-31
- Primary Completion
- 2018-12-31
- Completion
- 2018-12-31
Countries
- United States
Study Locations
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