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Phentermine/Topiramate for Uric Acid Stones
Sponsor: University of Florida
Summary
The investigator proposes an 18 month, feasibility pilot study, randomizing obese and diabetic individuals with pure uric acid nephrolithiasis (UAN) or mixed calcium oxalate (CO) UAN to either phentermine/topiramate or a pragmatic control group who will remain on their standard medication regimen (citrate salts, allopurinol, diet, etc.).
Official title: Phentermine/tOpiramate to eND Obesity and Uric Acid Stones Trial (POuND OUT)
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
19
Start Date
2021-03-31
Completion Date
2024-11-14
Last Updated
2026-06-15
Healthy Volunteers
No
Interventions
Phentermine / Topiramate Oral Product
All participants in the experimental group will receive oral generic tablet phentermine (18.75 or 37.5 mg dose) and topiramate (daily 100 mg or 150 mg dose)
Citrate Salts, Allopurinol, Diet
Control participants will complete initial visit requirements and study enrollment and will be maintained on their current therapy.
Locations (1)
University of Florida
Gainesville, Florida, United States