Oxalate-Driven Host Responses in Kidney Stone Disease
Launched by UNIVERSITY OF ALABAMA AT BIRMINGHAM · Jun 8, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how a substance called oxalate affects the development of kidney stones and the body's immune response. The researchers want to understand more about how this process works, so they are looking for both healthy participants and those who have calcium oxalate kidney stones. If you are between the ages of 18 and 60, not pregnant or breastfeeding, and meet other health criteria, you could be eligible to join the study.
Participants will participate for about three weeks, during which they will follow specific diets provided by the study team and provide blood and urine samples for testing. It’s important to note that participants will need to avoid certain supplements and vigorous exercise during the study. This research could help improve our understanding of kidney stones and potentially lead to better prevention and treatment options in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Men and women between the ages of 18 and 60 years old.
- • Able to provide informed consent.
- • BMI between 20-30 kg/m2.
- • Non-tobacco users or not pregnant/breastfeeding/nursing.
- • Normal fasting blood comprehensive metabolic panel, complete blood count, C-reactive protein, and urinalysis. Must accurately collect two 24-hour urine collections within 20% of the appropriate ratio of creatinine (mg)/body weight (kg) for respective gender.
- • Healthy subjects: No history of CaOx KS or other medical conditions.
- • Patients with CaOx KS: Recent stone composition \> 50% CaOx; no uric acid, struvite, or carbonate apatite stone content. Must be first-time or recurrent CaOx stone former (last stone event ≤ 3 years).
- • Willing to not consume supplements (i.e. vitamins, Ca (citrate or carbonate) and other minerals, herbal supplements, nutritional aids, and probiotics) for 2 weeks before the study and during the study.
- • Willing to abstain from vigorous exercise during the study as this may compromise immune function.
- • Willing to consume diets provided only by the UAB CCTS Bionutrition Core. No food allergies or intolerance to any of the foods on the study menus.
- • Willing to accurately collect 24-hour urine samples, and to have blood drawn throughout the study.
- • If on medications for KS prevention (e.g. thiazides, citrate supplementation excluding calcium citrate), patients must be on a stable dose regimen for at least 8 weeks prior to and during screening, with no changes in dosing anticipated during the study. Patients should not take allopurinol for 2 weeks prior to screening since allopurinol has antioxidant properties.
- Exclusion Criteria:
- • Failure to meet the inclusion criteria or physician refusal.
- • Inability to sign and read the informed consent.
- • Any medical, psychiatric, or social conditions that would prohibit participants from abiding by the study requirements.
- • BMI ˃30 kg/m2 and \<20 kg/m2
- • Tobacco users or pregnant or breastfeeding/nursing women.
- • Abnormal fasting blood comprehensive metabolic panel, complete blood count, C-reactive protein, and urinalysis. Inaccurate 24-hour urine collections.
- • Healthy subjects: Currently taking or have recently taken medications within the last 3 months (i.e. antibiotics) or dietary supplements. History of KS or any medical condition that could influence absorption or excretion of oxalate.
- • Active illness including COVID-19, flu, common cold, fever, diarrhea, urinary tract infections, or other infections 14 days before the study and throughout the study.
About University Of Alabama At Birmingham
The University of Alabama at Birmingham (UAB) is a prominent academic institution and research hub dedicated to advancing healthcare through innovative clinical trials. Renowned for its commitment to medical discovery and education, UAB conducts cutting-edge research across a wide array of disciplines, including oncology, cardiology, neurology, and public health. With a robust infrastructure for clinical research, UAB fosters collaboration among interdisciplinary teams, leveraging state-of-the-art facilities and resources to enhance the translation of scientific findings into effective treatments and interventions. As a leader in clinical research, UAB aims to improve patient outcomes and contribute to the broader medical community through rigorous trial design and implementation.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Birmingham, Alabama, United States
Patients applied
Trial Officials
Tanecia Mitchell, PhD
Principal Investigator
University of Alabama at Birmingham
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials