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RECRUITING
NCT06989320
NA

Endogenous Oxalate Synthesis in Idiopathic Calcium Oxalate Kidney Stone Disease

Sponsor: University of Alabama at Birmingham

View on ClinicalTrials.gov

Summary

The goal of this clinical trial study is to test if patients with idiopathic calcium oxalate kidney stones have an increased production of oxalate by the body, which would lead to increased urinary excretion of oxalate. The study will recruit adult patients with a history of calcium oxalate kidney stones and healthy volunteers without kidney stones. Participants will ingest fixed diets containing low amounts of oxalate for 5 days ingest a soluble form of glycolate and vitamin C collect urine, blood, stool during the dietary and oral dosing portions of the study and also collect breath sample during the oral glycolate test

Official title: Endogenous Oxalate Synthesis in Idiopathic Calcium Oxalate Kidney Stone Formers

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2025-05-27

Completion Date

2031-12-31

Last Updated

2025-05-31

Healthy Volunteers

Yes

Interventions

DIETARY_SUPPLEMENT

Low-oxalate diet and glycolate dosing

Low-oxalate diet 4 days of fixed eucaloric diet with low oxalate (\<60 mg/day), normal calcium content (600-1000 mg/day)

DIETARY_SUPPLEMENT

Oral glycolate dosing

Oral 13C-glycolate dosing (0.5 mg/kg)

DIETARY_SUPPLEMENT

Oral 13C- ascorbic acid dosing

Oral 13C- ascorbic acid dosing (0.75 mg/kg)

Locations (2)

United States, Alabama University of Alabama at Birmingham

Birmingham, Alabama, United States

University of Texas South Western Medical Center

Dallas, Texas, United States