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NAFLD clinical trials

View clinical trials related to NAFLD.

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NCT ID: NCT04845646 Completed - Healthy Clinical Trials

DDI Study of ASC41 in HV and the PK, Safety and Tolerability in Subjects With NAFLD.

Start date: March 16, 2021
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to evaluate the effect of itraconazole, a strong inhibitor)of cytochrome P4503A , and phenytoin a strong inducer of cytochrome P450 3A, CYP3A4, CYP1A2 and CYP2C19 on the pharmacokinetics of ASC41, a THR beta agonist tables in healthy subjects. The PK, Safety and Tolerability of ASC 41 in Subjects with NAFLD will also be evaluated. Approximately 24 subjects including 16 healthy volunteers (HVs) and 8 subjects with NAFLD will be enrolled. This study consists of 3 cohorts.

NCT ID: NCT04834063 Completed - NAFLD Clinical Trials

Serum Selenium and Zinc Levels in Non-alcoholic Fatty Liver Disease Patients

NAFLD
Start date: March 15, 2021
Phase:
Study type: Observational

Non-alcoholic fatty liver disease (NAFLD) includes a wide range of disorders that consist of simple fatty infiltration, steatohepatitis (NASH), and end-stage liver disease (cirrhosis). NAFLD is the most common cause of chronic liver disease worldwide and increases the risk of end-stage liver disease and hepatocellular carcinoma (HCC) . While risk factors such as obesity, diabetes, and a sedentary lifestyle may increase the risk of NAFLD, studies have shown that environmental exposures may further contribute to the pathogenesis of NAFLD. Although the pathogenic role of macronutrients is well established in both NAFLD and obesity, the contribution of micronutrients to NAFLD pathogenesis has garnered less attention than with obesity. Selenium is an essential element in many biological functions and is an important component of human nutrition. Exposure to selenium can be found in nature, such as rocks and sediment, air, soil, fuel oil, drinking water and nutritional supplementation. It is a major component of many enzymes such as glutathione peroxidase and plays an important role in anti-oxidation, DNA synthesis, reproduction, muscle function, and thyroid metabolism. Selenium concentrations have been studied in many diseases and organ systems including the liver. However, the exact relationship between selenium in patients with NAFLD is unclear. Selenium is an essential element in many biological functions and is an important component of human nutrition. It is a major component of many enzymes such as glutathione peroxidase and plays an important role in anti-oxidation, DNA synthesis, reproduction, muscle function, and thyroid metabolism. Selenium concentrations have been studied in many diseases and organ systems including the liver. However, the exact relationship between selenium in patients with NAFLD is unclear. Despite data suggesting mineral deficiencies in NAFLD patients, most data do not support insufficient mineral consumption as a possible mechanism for these deficiencies, except in the case of zinc deficiency. Zinc is the second most prevalent trace element in the body. It is integrally involved in the normal life cycle and has many important regulatory, catalytic, and defensive functions. Zinc deficiency occurs in many types of liver disease, especially more advanced/decompensated disease.

NCT ID: NCT04812262 Completed - Clinical trials for Overweight and Obesity

A Phase 1 Study of DD01 in Overweight/Obese Subjects With T2DM and NAFLD

Start date: February 24, 2021
Phase: Phase 1
Study type: Interventional

This is a Phase 1, first in human (FiH), randomized, double-blind, placebo-controlled, single ascending dose (SAD) and multiple ascending dose (MAD) study to investigate the safety, tolerability, PK and PD of DD01 administered by subcutaneous (SC) injection in overweight/obese subjects with type 2 diabetes (T2DM) and nonalcoholic fatty liver disease (NAFLD). The study will be conducted in 2 Parts (Part A and B), with up to 8 cohorts included in each part (Part A; Cohorts A1 to A8 and Part B; Cohorts B2 to B8).

NCT ID: NCT04779905 Completed - Clinical trials for Chronic Kidney Diseases

Chronic Kidney Disease and Non-alcoholic Fatty Liver Diseases

NAFLD
Start date: February 28, 2021
Phase:
Study type: Observational

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease worldwide. This disease reportedly affects up to 30% of the general population in Western countries, especially in patients with metabolic syndrome, obesity, and type II diabetes. NAFLD is considered to be an independent risk factor for cardiovascular disease and there is accumulating evidence to support a causative role in the development of chronic kidney disease (CKD). So, we aim first to assess the prevalence of chronic kidney disease in NAFLD patients, secondly to detect the association between hepatic fibrosis and CKD in NAFLD patients

NCT ID: NCT04704063 Completed - NAFLD Clinical Trials

Efficacy and Safety of Tocovid Suprabio 200mg in Non-alcoholic Fatty Liver (NAFL)

T3-NAFL
Start date: January 1, 2021
Phase: Phase 2
Study type: Interventional

Palm-derived tocotrienols have shown hepatoprotective effects in both animal and human studies. This study aims to investigate the effects of tocotrienols in hepatocellular lipid content using MRI. Non-alcoholic fatty liver disease (NAFLD) is a spectrum of diseases ranging from simple fatty liver (steatosis, NAFL) to non-alcoholic steatohepatitis (NASH) to cirrhosis. NASH is the accumulation of fat in liver cells accompanied with inflammation that can lead to the scarring of the liver. Prevention of liver fibrosis by early introduction of low risk interventions such as lifestyle modification, diet control and nutraceuticals may help circumvent long-term healthcare costs associated with management of chronic NASH.

NCT ID: NCT04692025 Completed - Healthy Clinical Trials

Study to Evaluate the Effect of Food on the Pharmacokinetics of ASC41 in Healthy Volunteers

Start date: December 27, 2020
Phase: Phase 1
Study type: Interventional

This study is to evaluate the effect of food on the pharmacokinetics of a single dose of ASC41 tablet in healthy volunteers, comparing fasting and postprandial pharmacokinetic parameters of Tmax, Cmax, AUC0-t, AUC0-∞.

NCT ID: NCT04686994 Completed - Clinical trials for Overweight and Obesity

Study to Evaluate the Safety and Efficacy of ASC41 in Overweight and Obese Subjects

Start date: December 22, 2020
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to evaluate the safety, tolerability and compare the pharmacokinetic parameters of ASC41, a THR beta agonist tables in overweight and obese subjects who have elevated LDL-C .

NCT ID: NCT04581421 Completed - Diabetes Clinical Trials

The Role of Dietary Carbohydrate and Fat Availability in the Regulation of Hepatic Lipid Content

LICARB
Start date: December 3, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate dietary compositions effect on liverfat measured by magnetic resonance imaging.

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: NCT04527965 Completed - Clinical trials for Diabetes Mellitus, Type 2

Liver Fat as a Dietary Target for Treating Cardiometabolic Disorders in Prediabetes and Type 2 Diabetes

NAFLDiet
Start date: August 11, 2020
Phase: N/A
Study type: Interventional

The overall aim of this study is to investigate the long-term impact of a customized diet aimed at reducing liver fat specifically and a healthy Nordic diet on ectopic fat (liver, pancreatic and visceral) and cardiometabolic risk in individuals with prediabetes and type 2 diabetes (T2D).