University of Missouri
Columbia, Missouri, 65212, United States
NCT Number: NCT03151798
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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Notify Me22 year–65 year
All sexes
Interventional
Not applicable
Columbia, Missouri, 65212, United States
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.
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
Exclusion criteria
Subjects will undergo energy restriction and exercise training over a 9 month period.
Subjects will receive dietary advice and receive information on a stretching program.
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
Time frame: 1 day
Liver tissue will be tested in vitro to determine the abundance of transcript indicative of fat oxidation.
Time frame: 1 day
Liver tissue will be tested in vitro to determine its capacity to burn fat
Time frame: 1 day
Liver samples will be tested to determine the severity of liver disease and whether diet and exercise reduce liver fibrosis.
University of Missouri-Columbia
Other
Nutrient Overload, Insulin Resistance, and Hepatic Mitochondrial Dysfunction
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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