Kidney Stone Inflammation
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Chicago
- Study ID
- NCT06436235
- Status
- Recruiting
Conditions
- Kidney Stone
- Stone, Kidney
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Accepted
Study Details
This observational study aims to look at the connections between kidney stones, insulin resistance, and inflammation. The researchers hypothesize that people who form calcium kidney stones and have insulin resistance may have higher levels of inflammation because they have more visceral fat (fat around the abdominal organs). The study will recruit 20 people who have had calcium kidney stones but don't have diabetes, and 20 healthy people who haven't had kidney stones. All the participants will come to the research center at the University of Chicago Medicine. Participants will have a dual-energy X-ray absorptiometry (DEXA) scan to measure their visceral fat, and give blood and urine samples. The blood will be tested for insulin resistance, inflammatory markers, and other metabolic factors. The urine will be analyzed for substances that increase kidney stone risk. The main goal is to see if the kidney stone formers with insulin resistance have more visceral fat compared to those without insulin resistance and the healthy participants. The researchers will also compare inflammatory marker levels between groups, and look at how visceral fat, inflammatory markers, insulin resistance, and urine stone risk factors are related. The findings may help explain how kidney stones are connected to metabolic conditions like diabetes and cardiovascular disease. Researchers hope this information will help identify stone formers at risk early and develop preventive treatments in the future.
Key Dates
- Start date
- Jun 30, 2024
- Status verified
- Sep 2025
- Primary completion
- May 1, 2026
- Completion
- Aug 1, 2026
Study Design
- Enrollment
- 40 participants (estimated)
Arms
- Arm: Kidney stone formersThe study team plans to enroll 20 non-diabetic participants with a history of at least one calcium-based kidney stone. Activities are the same for both cohorts, as follows: * Before clinic visit, participants will halt specific supplements and diuretics for a week. * At home, they complete a dietary questionnaire and collect 24-hour urine. * On the 7th day, they visit University of Chicago CRC. There, investigators will take measurements (height, weight) and DEXA scan, alongside kidney stone history review. * Throughout the day, participants provide urine and blood samples, undergo blood pressure checks, and fast until sample collection. * Samples undergo testing for kidney stone, inflammation, and diabetes risk factors and are stored for future research.
- Arm: Control cohortThe study team plans to enroll 20 healthy control participants with no history of kidney stones or family history of kidney stones. Activities are the same for both cohorts, as follows: * Before clinic visit, participants will halt specific supplements and diuretics for a week. * At home, they complete a dietary questionnaire and collect 24-hour urine. * On the 7th day, they visit University of Chicago CRC. There, investigators will take measurements (height, weight) and DEXA scan, alongside kidney stone history review. * Throughout the day, participants provide urine and blood samples, undergo blood pressure checks, and fast until sample collection. * Samples undergo testing for kidney stone, inflammation, and diabetes risk factors and are stored for future research.
Primary Outcome Measure
Difference in visceral fat content in participants who form kidney stones with insulin resistance compared to participants who form kidney stones without insulin resistance and controls [ Time Frame: 1 week total, one half day in the CRC ]
Central Contacts
- Megan Prochaska, MD773-702-1000
- Elaine Worcester, MD773-702-3630
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago Medical Center | Chicago | Illinois | 60637 | Megan Prochaska, MD (PRINCIPAL_INVESTIGATOR) |
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