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Prospective Research Rare Kidney Stones (ProRKS)
Sponsor: Mayo Clinic
Summary
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.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
220
Start Date
2016-05
Completion Date
2026-07
Last Updated
2025-08-06
Healthy Volunteers
No
Conditions
Locations (11)
University of Alabama @ Birmingham
Birmingham, Alabama, United States
Mayo Clinic Jacksonville
Jacksonville, Florida, United States
Children's Memorial Hospital
Chicago, Illinois, United States
Children's Hospital, Harvard Medical School
Boston, Massachusetts, United States
Mayo Clinic Hyperoxaluria Center
Rochester, Minnesota, United States
New York University
New York, New York, United States
Cincinnati Children's Hosptial Medical Center
Cincinnati, Ohio, United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Hosptial of Sick Children
Toronto, Ontario, Canada
Landspitali Universtiy Hospital
Reykjavik, Iceland
Shaare Zedek Medica Center
Jerusalem, Israel