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Clinical Trial Summary

In this study the investigators will quantitate hepatic mitochondrial fluxes in T2D patients with NAFL and NASH before and after 16-weeks treatment with the insulin sensitizer pioglitazone


Clinical Trial Description

The study team will examine hepatic mitochondrial TCA flux and pyruvate cycling (oral [U-13C]-propionate), hepatic gluconeogenesis (oral 2H2O), and hepatic insulin sensitivity (intravenous [3,4-13C2]-glucose with euglycemic insulin clamp) before and after 16 weeks treatment with the FDA approved insulin sensitizer pioglitazone. These studies will be performed in (i) type 2 diabetic subjects with NAFL but without evidence of fibrosis, and (ii) type 2 diabetic patients with NASH. Liver biopsies will be obtained before and after treatment for the diagnosis of NAFL/NASH and for molecular analyses. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05305287
Study type Interventional
Source The University of Texas Health Science Center at San Antonio
Contact Luke Norton, PhD
Phone 210-567-0739
Email nortonl@uthscsa.edu
Status Recruiting
Phase Phase 4
Start date November 1, 2022
Completion date March 31, 2027

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