RecruitingPhase 4NCT03878459

Dapagliflozin Plus Pioglitazone in T1DM

Can Addition of Pioglitazone to SGLT2 Inhibitor in Type 1 Diabetic Patients Amplify the Decrease in HbA1c and Prevent the Increase in Plasma Ketone Concentration?


Sponsor

The University of Texas Health Science Center at San Antonio

Enrollment

120 participants

Start Date

Aug 8, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

Purpose: To examine the effect of addition of combination therapy with dapagliflozin plus pioglitazone to insulin on glucose control and plasma ketone concentration in patients with type 1 diabetes (T1DM) Research Design: 120 patients with type 1 diabetes who otherwise are healthy constitute the study population. After screening, eligible subjects will start 4 week run in. At week 4, subjects will receive dapagliflozin for 12 weeks. At week 16, subjects will be randomized to receive in a double blind fashion pioglitazone or placebo for 16 weeks. Methods: the following techniques will be employed in the present study: (1) mixed meal tolerance test; (2) indirect calorimetry; (3) continuous glucose monitoring. Clinical Relevance: the results of the present study will demonstrate that the addition of pioglitazone to SGLT2 inhibitor in T1DM patients produces greater reduction in the HbA1c without increasing risk of ketoacidosis and hypoglycemia.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a combination of two diabetes drugs — dapagliflozin (an SGLT2 inhibitor) and pioglitazone — can help improve blood sugar control in adults with type 1 diabetes who are already on insulin but not reaching their target blood sugar levels. These drugs are typically used for type 2 diabetes but may offer benefits in type 1. **You may be eligible if...** - You are over 18 years old with type 1 diabetes - Your blood sugar control is suboptimal (HbA1c between 7.0% and 11.0%) - You use multiple daily insulin injections or an insulin pump - Your kidney function is adequate (eGFR at least 60) - Your weight has been stable for the past 3 months **You may NOT be eligible if...** - You have type 2 diabetes - Your kidney function is below the required level - You have blood in your urine - You are pregnant, breastfeeding, or planning to become pregnant Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPioglitazone 45 mg

patients will be started on 15 mg and the dose escalated to the maximal tolerated dose

DRUGPlacebo

PATIENTS WILL RECEIVE PLACEBO


Locations(3)

University Health System Texas Diabetic Institute

San Antonio, Texas, United States

Endocrinology and Diabetes Center, Rambam Medical Center

Haifa, Israel

Dasman Diabetes Institute

Kuwait City, Kuwait

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NCT03878459


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