Clinical Trials Logo

Fatty Liver clinical trials

View clinical trials related to Fatty Liver.

Filter by:

NCT ID: NCT01899859 Completed - Clinical trials for Non-Alcoholic Steatohepatitis (NASH)

Phase 1 Study to Evaluate Safety of GR-MD-02 in Subjects With Non-Alcoholic Steatohepatitis (NASH) and Advanced Fibrosis

Start date: July 2013
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to characterize the safety, tolerability and dose-limiting toxicities (DLTs) for GR-MD-02 when administered intravenously to subjects with biopsy-proven NASH with advanced liver fibrosis.

NCT ID: NCT01894438 Completed - Clinical trials for Non-alcoholic Steatohepatitis (NASH)

Mediterranean Lifestyle Intervention in Patients With Non-alcoholic Fatty Liver Disease

Start date: April 2013
Phase: N/A
Study type: Interventional

Non-alcoholic fatty liver disease (NAFLD) is considered as the hepatic manifestation of the metabolic syndrome. NAFLD is a pathologic condition which involves both hepatic steatosis and non alcoholic steatohepatitis (NASH), as the result of fat accumulation in the liver (liver fat >5-10% of liver weight), not due to excess alcohol consumption or other causes of steatosis. At present, no medication or surgical procedure has been approved for treating NAFLD and lifestyle modifications remain the cornerstone therapy targeting both at weight reduction for overweight subjects and at prevention of overweight for the normal weight individuals. Given that a Mediterranean dietary pattern has a beneficial effect both on the prevention and the resolution of the metabolic syndrome, the main aim of the present study is to implement and evaluate the potential benefits of an intervention based on the Mediterranean lifestyle in a sample of patients with NAFLD.

NCT ID: NCT01876108 Completed - Insulin Resistance Clinical Trials

The Effect of Helicobacter Pylori Eradication on Liver Fat Content in Non-alcoholic Fatty Liver Disease

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The role of Helicobacter pylori(HP)in the pathogenesis of non-alcoholic fatty liver disease (NAFLD) is controversial.

NCT ID: NCT01875978 Completed - Clinical trials for Non-alcoholic Fatty Liver Disease

Effect of Phytosterols on Nonalcoholic Fatty Liver Disease

Start date: October 2012
Phase: N/A
Study type: Interventional

Phytosterols are plant sterols . Phytosterols have anti-inflammation effect. Investigators have a hypothesis: phytosterols reduce oxidative stress , enhance Insulin-like growth factor-1(IGF-1) and endothelial progenitor cells(EPCs). Therefore, phytosterols has novel role in cardiovascular protection.

NCT ID: NCT01874249 Completed - Clinical trials for Non Alcoholic Fatty Liver Disease

Non Invasive Assessment of Liver Fibrosis in Fatty Liver Disease

Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this randomized clinical trial is to evaluate the utility of noninvasive markers for the detection of advanced fibrosis in patients newly diagnosed with Non-alcoholic Fatty Liver Disease (NAFLD) by ultrasound. The primary objective is to determine the effectiveness of noninvasive markers for detect of advanced fibrosis in patients with diagnosis of fatty liver disease. The secondary objectives are: - To determine the increase in health care with the specialist (gastroenterologist or endocrinologist). - To determine which noninvasive evaluation strategy favors any treatment of fatty liver disease.

NCT ID: NCT01828528 Completed - Clinical trials for Nonalcoholic Steatohepatitis

Impact of Bariatric Surgery on Nonalcoholic Fatty Liver Disease

Start date: April 2013
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the effect of weight loss rate on liver steatosis, steatohepatitis, fibrosis and cardiovascular risk at different stages before and after bariatric surgery. The investigators also aim to study the short-term effect of bariatric surgery on gastric cholecystokinin levels before and 10 days after the bariatric surgery.

NCT ID: NCT01817491 Completed - Obesity Clinical Trials

Low Fat Vegan or American Heart Association Diets & Cardiovascular Risk in Obese 9-18 y.o. With Elevated Cholesterol

Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the short-term effects of a reduced fat plant-based diet on biomarkers of inflammation, oxidative stress and cardiovascular risk. This plant-based diet consists of whole grains, fruits and vegetables and little amounts of nuts and seeds, with no limitations on the amount of food intake. Animal products are not allowed. The results of the plant-based diet will be compared with the diet recommended by American Heart Association. This diet also emphasizes fruits and vegetables, but allows healthy fats, low-fat meats, fish and low-fat dairy in moderation. The results of the study might be useful in understanding whether or not plant-based diets are protective against cardiovascular disease.

NCT ID: NCT01811472 Completed - Clinical trials for Non-alcoholic Fatty Liver Disease (NAFLD)

Study to Assess the Efficacy, Safety and Tolerability of LCQ908 in NAFLD Patients

Start date: June 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study was to determine whether LCQ908 effectively lowers liver fat, as assessed by MRI and to assess its safety and tolerability profile in subjects with non-alcoholic fatty liver disease (NAFLD).

NCT ID: NCT01798719 Completed - NAFLD Clinical Trials

Effect of Mediterranean Diet on Non-alcoholic Fatty Liver Disease

Nutriepa
Start date: February 2011
Phase: N/A
Study type: Interventional

Non-alcoholic fatty liver disease (NAFLD) is a clinical/biochemical condition associated with the metabolic syndrome. As the disease stems from excess calorie intake and lack of physical activity, the correction of unhealthy lifestyles is the background of any prevention and treatment strategy

NCT ID: NCT01792115 Completed - Fatty Liver Clinical Trials

Treatment for Non-Alcoholic Fatty Liver With Different Doses of Vitamin E

Start date: May 1, 2013
Phase: Phase 2
Study type: Interventional

Background: - Non-alcoholic fatty liver disease (NAFLD) is an excess accumulation of fat in the liver cells. It is associated with obesity, high blood pressure, high cholesterol, and diabetes. Some people with NAFLD only have excess fat in the liver. However, other people may develop a worse form of NAFLD with liver injury and scarring. This form, called non-alcoholic steatohepatitis (NASH), can lead to liver failure, liver cancer, and death. Not much is known about why some people develop NASH and others do not. - Lifestyle changes such as diet, exercise, and weight loss can decrease the liver damage in NAFLD. Some studies show that vitamin E can also help treat NAFLD. The dose of vitamin E used in these studies is almost 40 times the recommended amount of vitamin E intake from food. It is unclear whether a lower dose could achieve the same effect. Researchers also want to study how vitamin E works at different doses to treat NAFLD. Objectives: - To find out the most effective dose of vitamin E to treat NAFLD. - To gain a better understanding of how NAFLD and NASH develop, and predict who will respond to treatment. Eligibility: - Individuals at least 18 years of age with suggestion of non-alcoholic fatty liver disease. Design: - Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected. - For the first 12 weeks of the study, participants will meet with a nutritionist. They will have personalized diet and exercise plans. Treatment will be monitored with diaries and questionnaires to fill out at home. Participants will also wear a pedometer to measure physical activity. - After the 12-week period, participants will have a full physical examination with the following tests: - Blood tests - Glucose tolerance tests - Imaging studies (DEXA scan and magnetic resonance imaging) - Liver and fatty tissue biopsy - Two weeks after the tests, participants will start vitamin E treatment. They will take up to two pills a day, taken with fat-containing foods. - 4 weeks after starting treatment they will have a repeat full evaluation with imaging tests, blood work, and liver and fat biopsies. - Participants who are taking vitamin E will take it for up to 120 weeks. They will have monitoring visits every 8 to 12 weeks. At the end of 120 weeks, they will have another full evaluation, with imaging tests, blood work, and liver and fat biopsies.