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COMPLETED
NCT04621929
PHASE2

Phentermine/Topiramate for Uric Acid Stones

Sponsor: University of Florida

View on ClinicalTrials.gov

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

DRUG

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)

COMBINATION_PRODUCT

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