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Fatty Liver clinical trials

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NCT ID: NCT01547910 Completed - Clinical trials for Non-alcoholic Fatty Liver Disease

Effect of Supplementation of Fish Oil on Non-alcoholic Fatty Liver Disease in Children

Start date: August 2007
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate efficacy of fish oil (EPA/DHA) in children with non-alcoholic fatty liver disease.

NCT ID: NCT01529268 Completed - Clinical trials for Nonalcoholic Fatty Liver Disease (NAFLD)

Cysteamine Bitartrate Delayed-Release for the Treatment of NAFLD in Children

CyNCh
Start date: June 2012
Phase: Phase 2/Phase 3
Study type: Interventional

CyNCh is a multi-center, placebo-controlled clinical trial of children ages 8 to 17 years with biopsy-confirmed moderate to severe nonalcoholic fatty liver disease (NAFLD). The primary objective is to evaluate whether 52 weeks of treatment with cysteamine bitartrate delayed-release capsules will result in improvement in liver disease severity.

NCT ID: NCT01492283 Completed - Type 2 Diabetes Clinical Trials

Pathophysiological Implications of the Incretin Hormones in Patients With Liver Disease With and Without Diabetes

Start date: December 2011
Phase: N/A
Study type: Observational

The main objective of this study is to analyze the pathophysiological implications of glucagon and the incretin hormones in patients with liver disease (Non alcoholic fatty liver disease (NAFLD) or cirrhosis) with and without diabetes compared with healthy controls. The present study will contribute significantly to the understanding of the pathophysiology of liver disease and glucose metabolism. The final goal is that the results could pave the way for new treatment modalities for patients with liver disease.

NCT ID: NCT01477307 Completed - Obesity Clinical Trials

Dietary Intervention and Intestinal Microbiota in Non-alcoholic Fatty Liver

Start date: July 1, 2013
Phase: N/A
Study type: Observational

In patients with NAFLD/NASH, changes in liver lipid composition and function tests following a short dietary intervention are associated with changes in gut microbiota

NCT ID: NCT01476995 Completed - Hypertension Clinical Trials

Prognostic Indicators as Provided by the EPIC ClearView

GBMC
Start date: September 2010
Phase: N/A
Study type: Observational

The objective of this study is to determine whether the finger tip images captured by the EPIC ClearView device, when analyzed via the ClearView software, produce a Response Scale that characterizes trends consistent with known diagnoses identified by medical doctors. Specifically, the investigators hypothesize that the organ system involving any of a series of known active diagnoses will be identified in the EPIC ClearView Response Scale report with the intention of providing potential triage capabilities.

NCT ID: NCT01464801 Completed - Fatty Liver Clinical Trials

Resveratrol in Patients With Non-alcoholic Fatty Liver Disease

LIRMOI3
Start date: September 2011
Phase: N/A
Study type: Interventional

Non-alcoholic fatty liver disease (NAFLD) and fatty liver hepatitis (NASH) are very common in the Western world and strongly associated with obesity. No known effective treatment is known. From animal studies, it is known that the compound resveratrol perhaps has the potential to neutralize obesity-induced diseases. Resveratrol is already widely used as a food supplement though the precise effects are unknown. This project focuses on the effect of Resveratrol on fatty liver disease. The researchers plan to investigate the effects of Resveratrol or placebo treatment for 6 months on NAFLD/NASH in obese patients.

NCT ID: NCT01446276 Completed - Obesity Clinical Trials

Long-term Investigation of Resveratrol on Fat Metabolism in Obese Men With Nonalcoholic Fatty Liver Disease

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate potential metabolic effects of resveratrol in obese healthy men with non-alcoholic fatty liver disease. The investigators hypothesize that resveratrol will: - decrease hepatic very-low-density-lipoprotein-triglyceride (VLDL-TG) secretion - decrease liver fat content - increase insulin sensitivity The investigators will look at changes in: - lipid turnover (VLDL-TG kinetics, palmitate kinetics, indirect calorimetry) - liver fat content (MR liver spectroscopy) - insulin sensitivity (glucose kinetics during hyperinsulinaemic euglycaemic clamp) - body composition (DXA and MRI) - lipase activity and fat cell size (fat biopsy from abdominal and femoral adipose tissue)

NCT ID: NCT01431521 Completed - Clinical trials for Non-alcoholic Fatty Liver Disease

Study of Changes in Hepatic Fat Following Administration of MK-4074 and Pioglitazone Hydrochloride (MK-4074-008)

Start date: October 26, 2011
Phase: Phase 1
Study type: Interventional

This study will evaluate changes in liver fat content following multiple oral doses of MK-4074 and Pioglitazone Hydrochloride in adult males and females with fatty liver disease. The primary hypothesis of the study is that a multiple-dose administration of MK-4074 200 mg twice daily for 4 weeks results in a decrease in hepatic fat content with respect to placebo in adult male and female participants with hepatic steatosis (i.e., on order of 50% reduction in hepatic fat with respect to placebo is expected).

NCT ID: NCT01418027 Completed - Clinical trials for Non-alcoholic Fatty Liver Disease (NAFLD)

Combined Intensive and Conventional Exercise on Nonalcoholic Fatty Liver Disease (NAFLD)

Start date: August 2011
Phase: Phase 3
Study type: Interventional

The prevalence of NAFLD is 50-70% in obese people. A decrease of calorie intake and increase of physical activity are recommended as an effective approach for the prevention and treatment of NAFLD. However, the exercise model for NAFLD intervention is understudied. In the present study we aim to compare the effect of intensive and conventional exercise interventions on NAFLD.

NCT ID: NCT01399645 Completed - Type 2 Diabetes Clinical Trials

Study of Liraglutide Versus Insulin on Liver Fat Fraction in Patients With Type 2 Diabetes

LIRAINS
Start date: May 2011
Phase: Phase 2
Study type: Interventional

This study is conducted to test the hypothesis that in type 2 diabetic adults with fatty liver who are resistant to metformin, treatment with liraglutide in combination with metformin will cause an absolute reduction in liver fat superior to insulin-metformin treatment within a 3-month period, as measured by magnetic resonance imaging (MRI).