Neutral Phosphate for Kidney Stones
What You Need to Know Before You Apply
What is the purpose of this trial?
Kidney stones are common and often come back. One reason may be that some people with calcium stones have low phosphate levels in the blood and lose too much phosphate through the kidneys. They may also have high calcium in the urine, which raises the chance of forming stones. In older studies, high doses of phosphate supplements lowered urine calcium and appeared to reduce stone formation, but they sometimes caused stomach and bowel side effects, and phosphate is no longer used for stone prevention. This small pilot study will test a much lower dose of neutral phosphate (250 mg twice daily) for 2 weeks in adults with recurrent calcium oxalate kidney stones, high urine calcium, and low blood phosphate. Participants will collect a 24-hour urine sample and have blood drawn before and after the 2-week period. The study will look at whether the low dose reduces urine calcium and the risk of stone formation in urine. The results will help decide whether a larger study is warranted.
Are You a Good Fit for This Trial?
This trial is for adults who have had repeated calcium oxalate kidney stones, have high calcium in their urine, and low phosphate levels in their blood.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Neutral Phosphate
Trial Overview
The study tests if taking a low dose of neutral phosphate (250 mg twice daily for 2 weeks) can lower urine calcium and reduce the risk of new kidney stones. Participants provide urine and blood samples before and after treatment.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Participants receive 250 mg of oral neutral phosphate twice daily for 2 weeks, dispensed by the University of Chicago Investigational Drug Service. Urine calcium and related stone risk measures are collected by 24-hour urine collection and compared before and after the 2-week course. A coordinator calls at 1 week to check for side effects and adherence, and these are assessed again at the final study visit.
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Who Is Running the Clinical Trial?
University of Chicago
Lead Sponsor
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