pioglitazone
DrugAn insulin sensitizer and anti-diabetic agent. Participants will be started on 15 mg/day, increased to 30 mg/day at week 2 and then to 45 mg/day at week 4.
Other names: Actos
NCT Number: NCT05305287
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
Interested in participating?
Request Info18 year–80 year
All sexes
Interventional
Phase 4
Texas Diabetes Institute - University Health System, San Antonio, Texas, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
T2D with NAFL
Inclusion criteria
Exclusion criteria
T2D with NASH
Inclusion criteria
Exclusion criteria
An insulin sensitizer and anti-diabetic agent. Participants will be started on 15 mg/day, increased to 30 mg/day at week 2 and then to 45 mg/day at week 4.
Other names: Actos
Placebo for pioglitazone
Time frame: Baseline, week 16
Quantitated using a combine stable isotope approach before and after treatment with pioglitazone
Time frame: Baseline, Week 16
Mean absolute change from baseline in liver fat content by MRI-PDFF
Time frame: Baseline, Week 16
Mean change from baseline in body weight
Time frame: Baseline, Week 16
Mean change from baseline in lean and fat mass measured by DEXA
Time frame: Week 16
Percentage of Participants with ≥1 Point Decrease in Fibrosis Stage with No Worsening of NASH on Liver Histology
Time frame: Week 16
Percentage of Participants that Achieve a ≥2 Point Decrease in NAS on Liver Histology, with ≥1 Point Reduction in at Least 2 NAS Components
Time frame: Baseline, Week 16
Mean change from baseline in Fibrosis-4 (FIB-4), transient elastography (Fibroscan®), NAFLD fibrosis score (NFS), alanine transaminase (ALT) and aspartate transaminase (AST)
Time frame: Baseline, Week 16
Lipidomics will be carried out using mass-spectrometry methods
Time frame: Baseline, Week 16
Multimodal RNA-Seq and ATAC-Seq will be used to examine gene regulatory networks in liver samples
Contact information is provided by the study sponsor or research team.
Andrea Hansis-Diarte, MPH
CONTACT
Luke Norton, PhD
CONTACT
The University of Texas Health Science Center at San Antonio
Other
Quantitation of Hepatic Mitochondrial Fluxes in Humans With Nonalcoholic Fatty Liver Disease (NAFLD)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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