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Thiazolidinedione

Pioglitazone + Weight Loss for Kidney Stones

Phase 4
Recruiting
Led By Khashayar Sakhaee, MD
Research Sponsored by University of Texas Southwestern Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 weeks
Awards & highlights
Drug Has Already Been Approved
No Placebo-Only Group
Pivotal Trial

Summary

This trial tests the effects of Pioglitazone, weight loss, or both in overweight and obese patients with uric acid kidney stones. Pioglitazone helps the body use insulin better and reduces urine acid, while weight loss improves health and reduces the risk of stones.

Who is the study for?
This trial is for adults over 21 with a specific type of kidney stone (over 90% uric acid) who are overweight but weigh less than 165 kg. They should have normal kidney function and not be on certain medications or have conditions like chronic diarrhea, heart failure, or uncontrolled diabetes.
What is being tested?
The study tests the effects of Pioglitazone (a diabetes drug), weight loss, or both combined on patients with uric acid kidney stones. Participants will follow a fixed diet and be monitored through various medical assessments over a period of 24 weeks.
What are the potential side effects?
Pioglitazone may cause side effects such as liver issues, swelling in legs (pedal edema), heart failure symptoms worsening if pre-existing, and potential increased risk of bladder cancer.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Urine pH
Secondary study objectives
Uric acid
Urine Ammonium/Net Acid Excretion
Urine Net Acid Excretion/Sulphate

Awards & Highlights

Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

3Treatment groups
Experimental Treatment
Group I: Weight Loss, BehavioralExperimental Treatment1 Intervention
Weight loss following the Group Lifestyle Balance Program based on the Diabetes Prevention Program that utilizes cognitive behavioral strategies (goal setting, problem solving, self-monitoring, stimulus control),and provides written education materials to support health and nutrition behavior changes for weight management and disease prevention.
Group II: Pioglitazone Drug (including Placebo)Experimental Treatment1 Intervention
45 mg/day- one pioglitazone tablet once daily throughout the 24 weeks of the study
Group III: Pioglitazone + Weight LossExperimental Treatment1 Intervention
Pioglitazone 45 mg/day + Weight Loss following the Group Lifestyle Balance Program based on the Diabetes Prevention Program that utilizes cognitive behavioral strategies (goal setting, problem solving, self-monitoring, stimulus control),and provides written education materials to support health and nutrition behavior changes for weight management and disease prevention.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Weight Loss
2008
Completed Phase 3
~1570
Pioglitazone 45 mg
2000
Completed Phase 4
~960

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Pioglitazone, a PPARγ agonist, reduces overly acidic urine, thereby lowering the risk of uric acid stone formation. Weight loss through caloric restriction and increased physical activity improves metabolic health, reduces urinary calcium and oxalate excretion, and increases urinary citrate excretion. These treatments are important for kidney stone patients as they target the metabolic and urinary abnormalities that lead to stone formation, thereby reducing the risk and recurrence of kidney stones.
The impact of body mass index on quantitative 24-h urine chemistries in stone forming patients: a systematic review and meta-analysis.Increased production and reduced urinary buffering of acid in uric acid stone formers is ameliorated by pioglitazone.Weight loss intervention reduces the risk of kidney stone formation in a rat model of metabolic syndrome.

Find a Location

Who is running the clinical trial?

University of Texas Southwestern Medical CenterLead Sponsor
1,080 Previous Clinical Trials
1,056,259 Total Patients Enrolled
6 Trials studying Kidney Stones
792 Patients Enrolled for Kidney Stones
Khashayar Sakhaee, MDPrincipal Investigator - UTSW
Children's Medical Center of Dallas, The University of Texas Southwestern Medical Center At Dallas, UT Southwestern Medical Center-Zale Lipshy Campus
Shiraz University Of Medical Sci & Hlth Serv (Medical School)
Vet Affairs Medical Center (Residency)
4 Previous Clinical Trials
178 Total Patients Enrolled

Media Library

Pioglitazone (Thiazolidinedione) Clinical Trial Eligibility Overview. Trial Name: NCT04370093 — Phase 4
Kidney Stones Research Study Groups: Pioglitazone Drug (including Placebo), Weight Loss, Behavioral, Pioglitazone + Weight Loss
Kidney Stones Clinical Trial 2023: Pioglitazone Highlights & Side Effects. Trial Name: NCT04370093 — Phase 4
Pioglitazone (Thiazolidinedione) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04370093 — Phase 4
~5 spots leftby Jun 2025