24-Hydroxylase Deficiency and CYP24A1 Mutation Patient Registry
NCT03478761 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 600
Last updated 2026-03-20
Summary
You are being asked to take part in this research registry because you or your family member is suspected to have a 24-hydroxylase deficiency.
Conditions
- 24-hydroxylase Deficiency
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
David Sas, MD · Mayo Clinic
-
Peter Tebben, MD · Mayo Clinic
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-10-19
- Primary Completion
- 2030-12-31
- Completion
- 2030-12-31
Countries
- United States
Study Locations
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