Rare Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been officially diagnosed with one of these rare kidney conditions: Primary Hyperoxaluria, Dent Disease, Cystinuria, or APRT Deficiency.
- You have a family history of one of these conditions, meaning a brother or sister has been diagnosed with Primary Hyperoxaluria, Dent Disease, Cystinuria, or APRT Deficiency.
Who may not be able to join:
- You do not have any of the four conditions listed (Primary Hyperoxaluria, Dent Disease, Cystinuria, or APRT Deficiency) and do not have a close family member with one of these conditions.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Dawn S. Milliner, M.D., Primary Hyperoxaluria Registry - Mayo Clinic, Rochester, MN
Phone: 507-538-5995
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Establish and expand registries and collaborate with patient organizations for the rapid dissemination of knowledge
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.