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Fatty Liver clinical trials

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NCT ID: NCT04160949 Recruiting - Fatty Liver Clinical Trials

A Pilot Study to Explore the Role of Gut Flora in Fatty Liver

Start date: March 2, 2020
Phase:
Study type: Observational

This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records regarding Fatty Liver.

NCT ID: NCT04141592 Recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

Investigating Pathological Mechanisms in Non-alcoholic Fatty Liver Disease

Start date: February 19, 2019
Phase:
Study type: Observational

To identify key characteristics of the tissue resident and peripherally circulating immune-phenotype in addition to blood markers, metabolic profile, faecal and oral microbiota in non-alcoholic fatty liver disease

NCT ID: NCT04104282 Recruiting - Clinical trials for Non-alcoholic Fatty Liver Disease

the Role of plin5 in the Development of Nonalcoholic Fatty Liver Disease.

Start date: December 1, 2016
Phase:
Study type: Observational [Patient Registry]

To further clarify the role of sequence polymorphism in patatin-like phospholipid domain containing protein 3 in the development of nonalcoholic fatty liver disease.

NCT ID: NCT04101162 Recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

NAFLD Study: US vs Liver Biopsy

NAFLD
Start date: September 15, 2019
Phase: N/A
Study type: Interventional

Evaluate the diagnostic accuracy of the new ultrasound software vs hepatic histology, the current reference standard for the diagnosis of NAFLD and NASH in 20 obese patients (BMI> 30) candidates for laparoscopic bariatric surgery and / or cholecystectomy

NCT ID: NCT04081571 Recruiting - Insulin Resistance Clinical Trials

Prevalence of NAFLD and Correlation With Its Main Risk Factors Among Egyptian

Start date: April 1, 2019
Phase:
Study type: Observational

Getting a rough indicator about the prevalence of different grade of severity of NAFLD (NASH & liver fibrosis), and Correlate the severity of fatty liver with different serological risk factors of metabolic syndrome and diseases progression as well as the prevalence of hepatocellular carcinoma related to NAFLD with the use of ; nutritional assessment designed and conducted by the investigators in this research, simple blood test (lipid profile and blood sugar), and easy cheap non-invasive radiological tool as screening to predict NASH.

NCT ID: NCT04074889 Recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

The Effect of Probiotics on the Clinical Outcomes and Gut Microenvironment in Patients With Fatty Liver

Start date: August 30, 2019
Phase: N/A
Study type: Interventional

Fatty liver has been associated with high risk of progression to inflammation of the liver, liver cirrhosis (hardening of the liver), and eventually can lead to liver cancer. So far, the treatment for this condition involves controlling the cholesterol level in the body by practicing low fat diet and daily exercise. However, recently there has been evidence that alteration of the normal population of various types of bacteria that lives in the intestines may contributes to the development of fatty liver. Probiotics is a dietary supplement containing live bacteria that is formulated to change the composition and population of the bacteria in the intestines. It is postulated that by taking specifically formulated probiotics, the alteration of the intestinal bacteria may lead to improvement of the fatty liver, leading to better daily liver function. In this 6-month study, investigators would like to investigate the effectiveness of the probiotics in improving the liver function and in the treatment of the fatty liver. It will compare the fatty liver of patients who took the probiotics supplements compared to those who did not took it and see if there is any improvement.

NCT ID: NCT04060368 Recruiting - Clinical trials for Non-alcoholic Steatohepatitis (NASH)

Efficacy and Safety of Endoscopic Sleeve Gastroplasty Versus Laparoscopic Sleeve Gastrectomy in Obese Subjects With NASH

TESLA-NASH
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The primary objectives of this study are to evaluate the effect of ESG with OverStitch® system (Apollo Endosurgery, Austin, TX, USA) compared to LSG on 1) histological improvement in NASH; 2) all-cause mortality and liver-related outcomes In obese subjects with non-alcoholic steatohepatitis (NASH). Condition or disease: Non-alcoholic steatohepatitis (NASH) with or without fibrosis Intervention/treatment: ESG with OverStitch® system vs LSG

NCT ID: NCT04054310 Recruiting - Clinical trials for NASH - Nonalcoholic Steatohepatitis

Non-Invasive Quantification of Liver Health in NASH (N-QUAN)

Start date: August 5, 2020
Phase: N/A
Study type: Interventional

To evaluate, in patients with suspected NASH referred for liver biopsy, the diagnostic performance of CT1 at discriminating those with NAS≥4 & F≥2 from those without.

NCT ID: NCT04012242 Recruiting - Ultrasound Clinical Trials

Innovative Liver Elasticity, Attenuation, and Dispersion Ultrasound Study

iLEAD
Start date: June 15, 2019
Phase:
Study type: Observational

The objective of this study is: (1) to investigate the correlation of ultrasound parameters (SW speed, Dispersion slope, Attenuation value, Normalized Local Variance, Liver / Kidney Intensity Ratio) with the pathological parameters (fibrosis, intralobular inflammation, ballooning degeneration and steatosis); (2) to evaluate the diagnostic performance of SW speed for liver fibrosis, Dispersion slope for intralobular inflammation and Attenuation value for steatosis by comparison with the tissue diagnosis by liver biopsy.

NCT ID: NCT04012021 Recruiting - Pancreatic Cancer Clinical Trials

EXplanted LIver and Ex-vivo Pancreatic Specimen Evaluation by 7 TESLA MRI

EXLIPSE
Start date: May 24, 2019
Phase: N/A
Study type: Interventional

Aim of this study is to evaluate the correlation between the characteristics detected by the 7T MRI equipment and the histological composition of native explanted livers (group A), liver graft excluded for donation (group B) and surgical specimens of primary pancreatic tumour, which underwent pancreaticoduodenectomy (group C).