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Fatty Liver clinical trials

View clinical trials related to Fatty Liver.

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NCT ID: NCT04561895 Completed - NAFLD Clinical Trials

Adipokine Genetic Variations in predictingNAFLD Progression to NASH in Egyptian Patients

Start date: January 1, 2020
Phase:
Study type: Observational [Patient Registry]

Due to the limited data concerning Egyptian population. authors aimed to investigate the differentadipokine gene polymorphism related to non alcoholic fatty liver disease incidence, prognosis and progression to steotosis and also to find different related factors including obesitu, diabetes and liver enzymes level

NCT ID: NCT04561804 Completed - Weight Loss Clinical Trials

NAFLD and Liver Fibrosis in Obese Adolescents

NAFLD
Start date: December 1, 2018
Phase:
Study type: Observational [Patient Registry]

Nonalcoholic fatty liver disease (NAFLD) is a chronic liver disease resulting from excessive fat accumulation in the liver. Due to its close association with obesity, it has become the most common liver disease in children in the United States. NAFLD can result in progressive fibrosis and lead to end-stage liver disease. Best practices in management of pediatric NAFLD are not clearly defined. Our aim is to clarify the natural history of NAFLD in obese children after weight loss surgery compare to lifestyle intervention. Our secondary aim is to investigate the added value of elastography for the screening and diagnosis of NASH with fibrosis.

NCT ID: NCT04561245 Completed - Clinical trials for NASH - Nonalcoholic Steatohepatitis

ALT-801 in Healthy Overweight and Obese Volunteers to Study Safety and Tolerability

Start date: November 10, 2020
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the safety and tolerability in healthy overweight and obese volunteers administered single or multiple repeated doses of ALT-801. This study has 2 parts. Part 1 involves a single dose of ALT-801 taken as a subcutaneous (SC) injection and will be approximately 36 days in duration. Part 2 involves 12 doses of ALT-801, once a week for 12 weeks, as a SC injection and will be approximately 116 days in duration. Each participant will enroll in only one part.

NCT ID: NCT04559126 Completed - Clinical trials for NASH - Nonalcoholic Steatohepatitis With Liver Fibrosis

A Study of EDP-297 in Healthy Subjects

Start date: September 8, 2020
Phase: Phase 1
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled study. It will assess the safety, tolerability, and pharmacokinetics of orally administered single and multiple doses of EDP-297 in healthy adult subjects.

NCT ID: NCT04551716 Completed - Clinical trials for Metabolic-dysfunction-associated Fatty Liver Disease (MAFLD)

Noninvasive Assessment of Metabolic Associated Fatty Liver Disease (MAFLD) in Chinese Population

Start date: September 10, 2020
Phase:
Study type: Observational

Attenuation imaging (ATI) technology independently developed by Canon medical is a non-invasive examination technology for quantitative detection and analysis of liver steatosis. The technique is simple, rapid and quantitative diagnosis, and is suitable for screening and popularization of early liver steatosis in MAFLD. As noninvasive and effective detection measures of liver inflammation and liver fibrosis, SWD and SWE are more and more widely used in the quantitative diagnosis of liver inflammation and fibrosis. Therefore, ATI combined with SWD / SWE detection can quantitatively diagnose different pathological stages (steatosis, necrotizing inflammation and liver fibrosis) in the development of MAFLD, so as to provide an important basis for treatment.

NCT ID: NCT04546984 Completed - Clinical trials for Nonalcoholic Steatohepatitis (NASH)

Multiple Dose Safety, Tolerability, PK,PD and Food Effect Study of HEC96719 in Healthy Adult Subjects

Start date: September 14, 2020
Phase: Phase 1
Study type: Interventional

The Safety, Tolerability, Pharmacokinetic, Pharmacodynamics and Food Effect Study of HEC96719 in Healthy Subjects

NCT ID: NCT04546022 Completed - Clinical trials for Galactose Single Point (GSP), Residual Liver Function

GSP as an Novel Indicator for Residual Liver Function in Patients With Fatty Liver

GSP
Start date: July 5, 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective is to determine the galactose single point (GSP) cutoff values to discriminate subjects with different hepatic function. The secondary objective is to analyze the correlations between GSP and other hepatic function assessment methods among this trial subjects.

NCT ID: NCT04537780 Completed - Clinical trials for Non Alcoholic Steatohepatitis

Efficacy and Safety of Montelukast in Non Alcoholic Steatohepatitis (NASH)

Start date: August 20, 2019
Phase: Phase 4
Study type: Interventional

the current study is to evaluate the efficacy and safety of Montelukast in the treatment of patients with non-alcoholic steatohepatitis (NASH).

NCT ID: NCT04523584 Completed - Clinical trials for Non-Alcoholic Fatty Liver Disease

Ultrasound Quantification of Liver Fat

Start date: November 8, 2016
Phase:
Study type: Observational

The investigators plan a prospective study designed to evaluate the accuracy of a new ultrasound method for quantification of liver fat content.

NCT ID: NCT04521114 Completed - Clinical trials for Nonalcoholic Steatohepatitis (NASH)

Leronlimab (PRO 140) in Patients With Nonalcoholic Steatohepatitis

NASH
Start date: December 1, 2020
Phase: Phase 2
Study type: Interventional

This is a phase II study of of Leronlimab (PRO 140)-Humanized monoclonal antibody to CCR5 in patients with Nonalcoholic Steatohepatitis (NASH).