The Effective of Potassium Sodium Hydrogen Citrate in Treating Uric Acid Stones Using Gut Microbiota and Metabolomics.
Launched by CHENG CAO · Oct 31, 2023
Trial Information
Current as of July 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how a medication called potassium sodium hydrogen citrate can help patients with uric acid stones, which are a type of kidney stone. The researchers want to understand how this treatment affects the gut bacteria and the substances produced in the body (metabolites) after taking the medication. Participants will take the medication for three months and will need to provide samples of their blood, urine, and stool before and after the treatment to help the researchers learn more about how the medication works.
To be eligible for this trial, patients must have been diagnosed with uric acid stones through specific imaging tests like ultrasounds or CT scans. They should not have certain health issues, such as cancer or liver problems, and should not have taken specific medications like statins recently. Participants can expect to take the medication for three months and contribute samples for analysis, helping to uncover important information that might improve treatment for uric acid stones in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • All stone patients were diagnosed using urologic ultrasonography, kidney-ureter-bladder (KUB) X-ray, or abdominal computed tomography (CT). Stone samples were obtained through ureteroscopic lithotripsy (URSL), percutaneous nephrolithotomy (PCNL), or extracorporeal shock wave lithotripsy (ESWL). Stones were analyzed using an automated infrared spectroscopy system, LIIR-20 (Lanmode Scientific Instrument Co., Ltd., Tianjin, China), and the main components were determined based on the most abundant substances listed in the report, which were classified as pure or mixed uric acid stones (anhydrous uric acid content \>50%).
- Exclusion Criteria:
- • Patients with malignancy, chronic liver insufficiency, a history of statin use, and thyroid or parathyroid disease were excluded from the study. Similarly, individuals with a history of urolithiasis or dyslipidemia as well as those who had used statins were excluded from the control group. Participants were also excluded if they had taken antibiotics or immune suppressants within one month prior to fecal sampling, or had a history of chronic diarrhea or constipation, chronic enteritis, irritable bowel syndrome, gastrointestinal tumors or intestinal surgery.
About Cheng Cao
Cheng Cao is a dedicated clinical trial sponsor committed to advancing medical research and innovation. With a focus on fostering the development of novel therapies, Cheng Cao collaborates with a network of healthcare professionals, researchers, and institutions to design and execute high-quality clinical trials. The organization prioritizes patient safety and ethical standards while striving to deliver impactful solutions that address unmet medical needs. Through rigorous scientific inquiry and a patient-centered approach, Cheng Cao aims to contribute significantly to the future of healthcare.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Changshu City, Jiangsu, China
Patients applied
Trial Officials
Cheng Cao, MD
Principal Investigator
The Changshu Hospital Affiliated to Soochow University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported