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NCT Number: NCT05305287

Quantifying Hepatic Mitochondrial Fluxes in Humans

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

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Texas Diabetes Institute - University Health System, San Antonio, Texas, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

T2D with NAFL

Inclusion criteria

  • Confirmed T2D based on OGTT (2 h glucose ≥200 mg/dl).
  • Treated with diet, metformin, and/or sulfonylurea and in good general health determined by medical history, physical exam, and routine blood chemistries;
  • age = 18-80 years;
  • BMI = 25-40 kg/m2;
  • HbA1c = 7-10%; stable body weight (±4 pounds) over the preceding 3-months;
  • not taking any medication known to affect glucose metabolism other than antidiabetic medications.
  • Evidence of moderate/severe fatty liver (steatosis; grade S2/S3 on FibroScan corresponding to ≥10% fat on MRI-PDFF) and no/minimal hepatic fibrosis (grade F0/F1 on FibroScan).

Exclusion criteria

  • Alcohol consumption >14 units/week for women and >21 units/week for men.
  • Cirrhosis (fibrosis stage 4).
  • Type 1 diabetes and/or GAD positive subjects.
  • Subjects not drug naive or have been on metformin more than 3 months.
  • Presence of proliferative retinopathy.
  • Urine albumin excretion > 300 mg/day.
  • Evidence of other forms of chronic liver disease, including alcoholic liver disease, hepatitis B and C, primary biliary cholangitis, suspected/proven liver cancer and any other liver disease other than NAFLD.
  • History of NY Class III-IV heart failure

T2D with NASH

Inclusion criteria

  • Confirmed T2D based on OGTT (2 h glucose ≥200 mg/dl).
  • Treated with diet, metformin, and/or sulfonylurea and in good general health determined by medical history, physical exam, and routine blood chemistries;
  • age = 18-80 years;
  • BMI = 25-40 kg/m2;
  • HbA1c = 7-10%;
  • stable body weight (±4 pounds) over the preceding 3-months;
  • not taking any medication known to affect glucose metabolism other than antidiabetic medications.
  • Evidence of moderate/severe fatty liver (steatosis; grade S2/S3 on FibroScan corresponding to ≥10% liver fat on MRI-PDFF) and moderate/severe hepatic fibrosis (grade F2/F3 on FibroScan).

Exclusion criteria

  • Alcohol consumption >14 units/week for women and >21 units/week for men.
  • Cirrhosis (fibrosis stage 4).
  • Type 1 diabetes and/or GAD positive subjects.
  • Subjects not drug naive or have been on metformin more than 3 months.
  • Presence of proliferative retinopathy.
  • Urine albumin excretion > 300 mg/day.
  • Evidence of other forms of chronic liver disease, including alcoholic liver disease, hepatitis B and C, primary biliary cholangitis, suspected/proven liver cancer and any other liver disease other than NAFLD.
  • History of NY Class III-IV heart failure

Treatment and study plan

pioglitazone

Drug

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

Other

Placebo for pioglitazone

Primary outcomes

  1. Effect of pioglitazone on hepatic mitochondrial TCA cycle fluxes

    Time frame: Baseline, week 16

    Quantitated using a combine stable isotope approach before and after treatment with pioglitazone

Secondary outcomes

  1. Mean absolute change from baseline in liver fat content by magnetic resonance Imaging - Proton Density Fat Fraction (MRI-PDFF)

    Time frame: Baseline, Week 16

    Mean absolute change from baseline in liver fat content by MRI-PDFF

  2. Mean change from baseline in body weight

    Time frame: Baseline, Week 16

    Mean change from baseline in body weight

  3. Mean change from baseline in body composition

    Time frame: Baseline, Week 16

    Mean change from baseline in lean and fat mass measured by DEXA

  4. Quantitate the effect of pioglitazone on liver histology by improvement of fibrosis

    Time frame: Week 16

    Percentage of Participants with ≥1 Point Decrease in Fibrosis Stage with No Worsening of NASH on Liver Histology

  5. Quantitate the effect of pioglitazone on NAFLD Activity Score (NAS)

    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

  6. Examine the effect of pioglitazone on non-invasive markers of NAFLD

    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)

  7. Effect of pioglitazone on the hepatic lipidome

    Time frame: Baseline, Week 16

    Lipidomics will be carried out using mass-spectrometry methods

  8. Effect of pioglitazone on hepatic gene regulatory networks

    Time frame: Baseline, Week 16

    Multimodal RNA-Seq and ATAC-Seq will be used to examine gene regulatory networks in liver samples

Study contacts

Contact information is provided by the study sponsor or research team.

Andrea Hansis-Diarte, MPH

CONTACT

[email protected]

210-567-3208

Luke Norton, PhD

CONTACT

[email protected]

210-567-0739

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center at San Antonio

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Official study title

Quantitation of Hepatic Mitochondrial Fluxes in Humans With Nonalcoholic Fatty Liver Disease (NAFLD)

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Mar 31, 2022
Registry last updated
Jan 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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