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Completed

NCT Number: NCT03151798

The Liver Health Study for Patients with NAFLD

The study will investigate whether the level of fat stored in the liver is related to the liver's ability to burn fat.

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Key information

Age range

22 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Missouri

Columbia, Missouri, 65212, United States

About this study

The study has two phases. In Phase I, liver samples from patients undergoing bariatric surgery or a diagnostic liver biopsy will be tested for the ability to burn fatty acids. In Phase II, patients with nonalcoholic fatty liver disease will participate in either a nine-month lifestyle treatment program or undergo standard care. The goal is to determine how weight loss and exercise improve liver health.

Inpatient comprehensive metabolic tests are performed before and after the nine-months.

Who can participate

Healthy volunteers accepted: No

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

For Phase I: Any patient scheduled to undergo bariatric surgery or a liver biopsy to diagnose nonalcoholic fatty liver disease.

For Phase II: Only subjects who have had a diagnosis of nonalcoholic fatty liver disease and completed Phase I (and no subjects who have undergone bariatric surgery)

Inclusion criteria

  • Men and women (pre and post-menopausal)
  • Overweight/obese with BMI ≥ 25.9 or < 50.0 kg/m2
  • Characteristics of the metabolic syndrome, pre-diabetes (fasting glucose 100-125 mg/dL or 2h glucose 140-200 mg/dL) or diabetes type 2, or undergoing bariatric surgery
  • 22-65 years of age
  • Sedentary, < 60 minutes per week of structured physical activity
  • Alcohol intake< 20 g/d

Exclusion criteria

  • Having undergone bariatric surgery.
  • Acute disease or advanced cardiac or renal disease, anticoagulation therapy, or any severe co-morbid condition limiting life expectancy < 1 years
  • Other causes of hepatitis including hepatitis B & C, autoimmune hepatitis, hemochromatosis, celiac disease, Wilson's disease, alpha-1-antitrypsin deficiency, medication-induced hepatitis, any clinical or biochemical evidence of decompensated liver disease
  • Use of steroids or other drugs that cause NAFLD
  • Pregnant or trying to become pregnant
  • Inability to exercise on a bike or treadmill

Treatment and study plan

Phase II: Lifestyle treatment

Behavioral

Subjects will undergo energy restriction and exercise training over a 9 month period.

Phase II: Control treatment

Behavioral

Subjects will receive dietary advice and receive information on a stretching program.

Phase I: Observational studies

Other

The liver samples from patients undergoing bariatric surgery or a diagnostic liver biopsy will undergo in vitro assays to determine the capacity of the tissue to burn fat

Primary outcomes

  1. Liver mitochondrial gene expression

    Time frame: 1 day

    Liver tissue will be tested in vitro to determine the abundance of transcript indicative of fat oxidation.

Secondary outcomes

  1. Liver mitochondrial fat oxidation

    Time frame: 1 day

    Liver tissue will be tested in vitro to determine its capacity to burn fat

  2. Histology to determine the amount of fibrosis in the liver

    Time frame: 1 day

    Liver samples will be tested to determine the severity of liver disease and whether diet and exercise reduce liver fibrosis.

Sponsors and collaborators

Lead sponsor

University of Missouri-Columbia

Other

Registry information

Official study title

Nutrient Overload, Insulin Resistance, and Hepatic Mitochondrial Dysfunction

Important dates

Study start
2017
Primary completion
2022
Study completion
2023
First posted
May 12, 2017
Registry last updated
Dec 19, 2024

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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