Protocol l: SGLT2 Inhibitors, Ketogenesis, and Ketoacidosis

Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

In this study, we will test the hypothesis that distinct mechanisms account for the SGLT2i-induced stimulation of ketogenesis and lipolysis versus endogenous (hepatic) glucose production in patients with type 2 diabetes (T2D) and type 1 diabetes (T1D), and that the increases in ketone production and lipolysis can be prevented by concomitant administration of the thiazolidinedione pioglitazone. We will conduct five distinct experiments to test this hypothesis in patients with T2D and T1D. MAIN STUDY: To examine the effect of empagliflozin versus empagliflozin/pancreatic clamp on EGP (6,6, D2-glucose), gluconeogenesis (D2O), lipolysis (U-2H-glycerol), ketogenesis (13C-palmitate conversion to 3-betahydroxybuyrate), and norepinephrine turnover (3H-NE) in type 2 diabetes subjects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 30
Maximum Age: 75
Healthy Volunteers: f
View:

• Ages 30-75 years

• Body Mass Index (BMI) 21-45 kg/m2

• Hemoglobin A1C (HbA1c) = 7.0-11%

• Estimated glomerular filtration rate (eGFR) \> 60 ml/min/1.73m2

• Blood Pressure (BP) \< 160/90 mmHg

• Participants must be in general good health based on medical history, physical exam, screening blood chemistries, complete blood chemistry (CBC), thyroid stimulating hormone/thyroxine (TSH/T4), electrocardiogram (EKG), and urinalysis

• Stable body weight (±1.5 kg) over the last 3 months and must not participate in an excessively heavy exercise program

• Patients treated with diet, sulfonylurea (SU), metformin (MET), or SU/MET

• Statin therapy is permissible if the dose has been stable for at least 3 months

Locations
United States
Texas
Texas Diabetes Institute/UH
RECRUITING
San Antonio
Contact Information
Primary
Ralph DeFronzo, MD
defronzo@uthscsa.edu
210-567-6691
Backup
Aurora Merovci, MD
merovci@uthscsa.edu
210-567-6691
Time Frame
Start Date: 2023-10-05
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 30
Treatments
Experimental: Empagliflozin
Empagliflozin 25 mg/day
Placebo_comparator: Placebo/Control Group
Placebo control
Sponsors
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Leads: The University of Texas Health Science Center at San Antonio

This content was sourced from clinicaltrials.gov