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Study identifier: NCT02780297 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prospective Research Rare Kidney Stones (ProRKS)

Condition: Hyperoxaluria · Cystinuria · Dent Disease  ·  Sponsor: Mayo Clinic

PhaseN/A
Planned participants220
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to determine the natural history of the hereditary forms of nephrolithiasis and chronic kidney disease (CKD), primary hyperoxaluria (PH), cystinuria, Dent disease and adenine phosphoribosyltransferase deficiency (APRTd) and acquired enteric hyperoxaluria (EH). The investigator will measure blood and urinary markers of inflammation and determine relationship to the disease course. Cross-comparisons among the disorders will allow us to better evaluate mechanisms of renal dysfunction in these disorders.

This description comes directly from the study's public registry record.

Talk to the study team

Barb Seide  ·  800-270-4637  ·  RareKidneyStones@mayo.edu

Julie Olson, RN  ·  800-270-4637  ·  RareKidneyStones@mayo.edu

Always discuss trial participation with your own doctor first.

Locations (11)

University of Alabama @ BirminghamBirmingham, Alabama, United StatesNot Yet Recruiting
Mayo Clinic JacksonvilleJacksonville, Florida, United StatesNot Yet Recruiting
Children's Memorial HospitalChicago, Illinois, United StatesNot Yet Recruiting
Children's Hospital, Harvard Medical SchoolBoston, Massachusetts, United StatesNot Yet Recruiting
Mayo Clinic Hyperoxaluria CenterRochester, Minnesota, United StatesRecruiting
New York UniversityNew York, New York, United StatesNot Yet Recruiting
Cincinnati Children's Hosptial Medical CenterCincinnati, Ohio, United StatesNot Yet Recruiting
Children's Hospital of PhiladelphiaPhiladelphia, Pennsylvania, United StatesNot Yet Recruiting
Hosptial of Sick ChildrenToronto, Ontario, CanadaNot Yet Recruiting
Landspitali Universtiy HospitalReykjavik, IcelandNot Yet Recruiting
Shaare Zedek Medica CenterJerusalem, IsraelNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT02780297