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Liver Fibrosis clinical trials

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NCT ID: NCT03896607 Terminated - Liver Fibrosis Clinical Trials

Liver and the Spleen Stifness in Adult Patients With Gaucher's Disease Using Ultrasound Shear Wave Elastography

Start date: March 30, 2019
Phase:
Study type: Observational

The investigated cohort will examine liver and spleen fibrosis in patients with Gaucher Disease(GD) by using Shear Wave Elastography- SWE to evaluation fibrosis of the tissue and to check the correlation of fibrosis with the biomarkers of disease severity.

NCT ID: NCT03539757 Terminated - Liver Fibrosis Clinical Trials

Development of Novel MRI Methods for Detecting, Discriminating, and Measuring Liver Fibrosis and Congestion in Fontan Patients

Start date: May 9, 2018
Phase:
Study type: Observational

In this research study, the investigators will conduct a prospective cross-sectional study of pediatric and adult Fontan patients that will correlate a variety of quantitative MRI biomarkers with histopathologic data.

NCT ID: NCT03479125 Terminated - Liver Cirrhosis Clinical Trials

Post-Treatment Follow-up Study for Liver Disease Subjects With or Without Cirrhosis After Receiving Emricasan or Placebo

Start date: February 27, 2018
Phase:
Study type: Observational

A post-treatment follow-up observational study for liver disease subjects with or without liver cirrhosis after receiving emricasan or placebo. Subjects must have been enrolled in a prior IDN-6556 study to be eligible.

NCT ID: NCT03352882 Terminated - Portal Hypertension Clinical Trials

Impact of Transjugular Intrahepatic Portosystemic Shunts on Liver Stiffness

Start date: August 2016
Phase: N/A
Study type: Interventional

Pilot study examining changes in liver stiffness measured by ultrasound before and after TIPS creation

NCT ID: NCT03027700 Terminated - Hepatic Steatosis Clinical Trials

Methods to Detect Liver Fibrosis

Start date: January 26, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to learn more about liver fibrosis and methods to detect it. We will evaluate and compare multiple MRI based measures of liver fibrosis in subjects with and without liver disease.

NCT ID: NCT01672879 Terminated - Clinical trials for Liver Fibrosis Due to NASH

Simtuzumab (SIM, GS-6624) in the Treatment of Cirrhosis Due to NASH

NASH
Start date: October 29, 2012
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the safety and efficacy of SIM (formerly referred to as GS-6624) in adults with compensated cirrhosis due to Non-Alcoholic Steatohepatitis (NASH). It will consist of 2 phases: - Randomized Double-Blind Phase - Open-Label Phase (optional)

NCT ID: NCT01672866 Terminated - Clinical trials for Liver Fibrosis Due to NASH

Safety and Efficacy of Simtuzumab (SIM, GS-6624) in Adults With Advanced Liver Fibrosis But Not Cirrhosis Secondary to Non-Alcoholic Steatohepatitis (NASH)

Start date: December 5, 2012
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate whether SIM (formerly referred to as GS-6624) is effective at preventing the histologic progression of liver fibrosis and the clinical progression to cirrhosis in participants with NASH. It will consist of 2 phases: - Randomized Double-Blind Phase - Open-Label Phase (optional)

NCT ID: NCT01341106 Terminated - Clinical trials for Hepatitis B, Chronic

Induction of Fibrosis Regression on Patients With Chronic Hepatitis B Infection

INFIRE
Start date: April 2011
Phase: Phase 4
Study type: Interventional

This study will examine whether 12 month treatment with entecavir(Baraclude®) has an effect on changes of liver stiffness measurement (LSM) and of hyaluronan measurement in patients with chronic hepatitis B infection.

NCT ID: NCT00453869 Terminated - Liver Fibrosis Clinical Trials

Screening of Fibrosing and/or Viral Chronic Hepatopathies in Jail

SNIFF11
Start date: April 2007
Phase: N/A
Study type: Observational

The prevalence of chronic hepatopathies is high in jail. However, the medical care of these hepatopathies is few developed. This study is an observational, an epidemiologic (screening and prevalence of fibrosing hepatopathies) and an evaluating study for a better taking care of these hepatopathies in jail. The aims of the study will be to evaluate the diagnostic performance of the FibroMeter score in the screening of the hepatic fibrosis in persons with multiple risk factors for liver fibrosis (alcoholism, intravenous drug users, tattoo, and virological status) with FibroScan® as gold standard; to evaluate the feasibility of these different screening tools for chronic hepatopathies in jail and to evaluate the prevalence of the fibrosing hepatopathies with clinically significant fibrosis and theirs risk factors, alcohol and hepatitis B and hepatitis C viruses in population from Angers jail.

NCT ID: NCT00151671 Terminated - Clinical trials for Hepatocellular Carcinoma

Effect of a Perioperative Oral Nutritional Supplementation on Patients Undergoing Hepatic Surgery for Liver Cancer

IMPACT
Start date: April 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Cirrhotic patients undergoing hepatic resection have a mortality rate near 10%, and 30 to 70% of them develop severe complications. These failures are mainly due to hepatic insufficiency. Studies have already shown benefits of oral nutritional supplements in ORL, digestive, and cardiac surgery. We aimed to ascertain whether this nutritional, immune-enhancing supplementation, administered 7 days before and 3 days after surgery, could improve liver function and postoperative host defences in patients with liver cancer resection.