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View Clinical Trial (Medical Research Study)


Exercise Versus Diet in the Treatment of Nonalcoholic Fatty Liver Disease

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City:   Columbia
State:   Missouri
Zip Code:   65212
Conditions:   Non Alcoholic Fatty Liver Disease
Purpose:   The central hypothesis of this proposal is that a reduction in hepatic mitochondrial function is the main pathophysiology behind NAFLD (Non-Alcoholic Fatty Liver Disease) and NASH (Non alcoholic steatohepatitis). The investigators further hypothesize that lifestyle modifications through aerobic exercise training without weight loss or diet-induced weight loss are effective in reducing NAFLD parameters by improving hepatic mitochondrial content and function in human subjects. The investigators propose a randomized, controlled human clinical trial to compare the effects of aerobic exercise training (without weight loss) versus diet-induced weight loss (without exercise) in individuals who have NAFLD or liver biopsy-confirmed NASH
Study Summary:   Fatty Liver Disease) and NASH (Non alcoholic steatohepatitis). The investigators further hypothesize that lifestyle modifications through aerobic exercise training without weight loss or diet-induced weight loss are effective in reducing NAFLD parameters by improving hepatic mitochondrial content and function in human subjects. The investigators propose a randomized, controlled human clinical trial to compare the effects of aerobic exercise training (without weight loss) versus diet-induced weight loss (without exercise) in individuals who have NAFLD or liver biopsy-confirmed NASH
Criteria:   Inclusion Criteria: - sedentary individual between - age group 18-60 years old - elevated Liver Function Tests (LFT's) with fatty liver on ultrasound and biopsy proven NASH Exclusion Criteria: - significant history of alcohol consumption > 20 gm/day (> 2 drinks / day) - evidence of other causes of hepatitis including positive screening B & C, autoimmune hepatitis, hemochromatosis, celiac disease, Wilson's disease, alpha 1 antitrypsin deficiency or medication-induced hepatitis - Subjects with planned exercise > 30-60 minutes per week - BMI < 25 or > 44 kg/m2 - clinical or biochemical evidence of decompensated liver disease, advanced cardiac or renal disease - changes in last 3 months the dose of oral hypoglycemic medication and statin, - positive stress test - pregnant women - demented individuals who cannot give consent
NCT ID:   NCT01327443
Primary Contact:   Principal Investigator
Jamal Ibdah, MD; PhD
University of Missouri-Columbia

Abhishek Choudhary, MD
Phone: 573 882 7349
Email: choudharya@health.missouri.edu
Backup Contact:   Email: rectors@health.missouri.edu
Scott Rector, PhD
Phone: 573 882 7349
Location Contact:   Columbia, Missouri 65212
United States



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Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   June 18, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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