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Fatty Liver clinical trials

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NCT ID: NCT03172650 Recruiting - Liver Diseases Clinical Trials

Effect of Non-alcoholic Fatty Liver Disease on Kidney Functions

Start date: July 1, 2017
Phase: N/A
Study type: Observational

Non-alcoholic fatty liver disease is the most common cause of chronic liver disease worldwide. It is defined as the accumulation of fat (>5%) in the liver cells in the absence of excessive alcohol intake or other causes of liver disease including viral, drug-induced, or autoimmune. Non-alcoholic fatty liver disease is a hepatic manifestation of metabolic syndrome.

NCT ID: NCT03151473 Recruiting - Clinical trials for Non-Alcoholic Steatohepatitis (NASH)

Longitudinal Observational Study Of Chinese With NAFLD/NASH

Start date: May 8, 2017
Phase:
Study type: Observational

This is a 10-year, longitudinal, observational study of patients with NAFLD/NASH designed to specifically address important clinical questions that remain incompletely answered from registration trials. In addition to the study database, the biospecimen repository will also be included so that translational studies of genomics and biomarkers of response may be performed.

NCT ID: NCT03142698 Recruiting - MRI Clinical Trials

Evaluation of 4 MRI Methods (PDFF 3, 6 and 11 Gradient Echoes and Spectroscopy) Compared to the Reference Method (Liver Biopsy) in Quantification of Hepatic Steatosis

STEA-MRI
Start date: May 2017
Phase: N/A
Study type: Interventional

Evaluation of 4 MRI methods (PDFF 3, 6 and 11 gradient echoes and Spectroscopy) compared to the reference method (liver biopsy) in quantification of hepatic steatosis

NCT ID: NCT03128918 Recruiting - Clinical trials for Non-alcoholic Fatty Liver Disease

Non-invasive Diagnosis of Non-alcoholic Steatohepatitis in Liver Transplant Recipients

Start date: July 2015
Phase: N/A
Study type: Observational

The purpose of this study is is to use non-invasive diagnostic tests, Fibroscan and a simple blood test, to diagnose NASH in patients who undergo liver transplantation. Liver transplantation is a life-saving procedure for people with cirrhosis. Fatty liver is a common reason for liver transplantation due to obesity and diabetes. Fatty liver can happen again to the new transplanted liver and it is often due to metabolic risk factors (including diabetes, rapid weight gain, and immunosuppressive therapy, which are used to avoid rejection of the new liver). Some patients with fatty liver after liver transplant have non-alcoholic steatohepatitis (NASH) injury to liver the tissue (inflammation) and damage which is caused by a build-up of fat in the liver. This is a serious problem and can lead to cirrhosis and loss of the transplanted liver. There has been no detailed study into the recurrence of NASH. One reason for this is one of the only ways to detect fatty liver and NASH is to have a liver biopsy, which can be painful and have complications. Recently, a new technology (Fibroscan) and a simple blood test (cytokeratin 18) have been developed which can tell doctors how much a liver is damaged and how much fat it contains without pain or complications. This is a year long study involving one screening visit and 3 study visits, 3 months apart.

NCT ID: NCT03073343 Recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

A Prospective, Randomized, Open Label Trial of Two Doses of Oral Betaine

Start date: November 12, 2013
Phase: N/A
Study type: Interventional

Betaine (trimethyglycine) is a food supplement that is approved for sale in the United States without a prescription. In this study, betaine will be provided to patients as a powder that can be mixed with aqueous solutions and consumed orally.

NCT ID: NCT03025074 Recruiting - Hepatitis C Clinical Trials

Blood Collection Biorepository for Liver Disease Research

Start date: July 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of establishing a biorepository is to provide high quality specimens (serum, plasma, buffy coat and liver tissue) for future researchers who are studying the effects that fatty liver and viral diseases have on the liver.

NCT ID: NCT02863757 Recruiting - Chronic Hepatitis B Clinical Trials

Follow-up of Chronic Hepatitis B Patients With Comorbid Nonalcoholic Fatty Liver Disease

Start date: August 2016
Phase:
Study type: Observational

The purpose of this study is to determine the disease progression in CHB/NAFLD compared with CHB and NAFLD including liver cirrhosis, cirrhotic complications and hepatocellular carcinoma (HCC).

NCT ID: NCT02815891 Recruiting - Clinical trials for Nonalcoholic Steatohepatitis

A Longitudinal Observational Study of Patients With Nonalcoholic Steatohepatitis (NASH) and Related Conditions Across the Entire Spectrum of Nonalcoholic Fatty Liver Disease (NAFLD)

Start date: July 2016
Phase:
Study type: Observational [Patient Registry]

TARGET-NASH is a longitudinal observational cohort study of patients being managed for NASH and related conditions across the entire spectrum NAFLD in usual clinical practice. TARGET-NASH is a research registry of patients with NAFL or NASH within academic and community real-world practices maintained in order to assess the safety and effectiveness of current and future therapies.

NCT ID: NCT02792634 Recruiting - Obesity Clinical Trials

Pathogenesis of Non-alcoholic Steatohepatitis and Liver Regeneration After Bariatric Surgery

NALKOSTEP
Start date: June 2016
Phase: N/A
Study type: Observational

Obesity and obesity related health problems are globally recognized as one of the major threats to public health. Bariatric surgery is the most effective and durable therapy option for obesity and the improvement of obesity related co-morbidities. "Non alcoholic steatohepatitis" (NASH) is an important comorbidity of obesity and improves after surgical intervention. In this study investigators try to enlighten the weight independent mechanism for the effects of bariatric surgery. Patients who are assigned to a bariatric procedure will be observed for at least 24 month. A liver and adipose tissue samples are gained during the operation. Liver function and morphology are observed before and after operation with LiMAx, FibroScan and ultrasound. Systemic inflammation is measured in blood samples before and after surgical intervention. In order to check the microbiome stool samples are collected throughout the entire observation period.

NCT ID: NCT02764047 Recruiting - Clinical trials for Non-alcoholic Fatty Liver Disease

Probiotics in the Treatment of NAFLD

Start date: January 2015
Phase: N/A
Study type: Interventional

Evaluate the effect of supplementation of probiotics on liver changes (histological and enzymatic), lipid profile and gut microbiota of patients with nonalcoholic steatohepatitis (NASH).