Clinical Trials Logo

Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

Filter by:

NCT ID: NCT02135536 Completed - Clinical trials for Primary Biliary Cirrhosis

Phase 2b Study of NGM282 Extended Treatment in Patients With Primary Biliary Cirrhosis

Start date: May 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, and activity of extended treatment with NGM282 in patients with Primary Biliary Cirrhosis.

NCT ID: NCT02134626 Completed - Liver Cirrhosis Clinical Trials

Simvastatin Effect on Portal Hypertension

Start date: August 2010
Phase: Phase 3
Study type: Interventional

It´s a clinical research of the effects in portal hypertension caused by simvastatin. We are going to use the hepatic venous pressure gradient(HVPG) measurement and the azygos flow at echoendoscopy to evaluate the benefits of the drug. Preliminary studies demonstrated that simvastatin can lower portal pressure.

NCT ID: NCT02132962 Completed - Cirrhosis Clinical Trials

Sarcopenia and Cirrhosis

Start date: May 2014
Phase: N/A
Study type: Interventional

The study investigates the effect of aminoacid infusion on proteinturnover in muscle from cirrhosis subjects, compared to healthy controls. The hypothesis is that aminoacid infusion can attenuate the increase in proteindegradation that follows cirrhosis.

NCT ID: NCT02132351 Completed - Cirrhosis Clinical Trials

Hepatic Fibrosis Non-invasive Methods Questionnaire

Start date: August 2013
Phase: N/A
Study type: Observational

Due to the limitations and the invasive nature of liver biopsy, there has been extensive interest in developing non-invasive tests to measure liver fibrosis (1). These are alternatives to liver biopsy that can be used in clinical practice, with benefits in terms of cost, risk, and patient convenience (2). Clinically applicable non-invasive tests include radiological studies, transient elastography (TE), and serum markers. We aim at studying acceptability, reliability, applicability and practical aspects of invasive and noninvasive methods for assessment of hepatic fibrosis and cirrhosis among hepatologists.

NCT ID: NCT02131831 Recruiting - Cirrhosis Clinical Trials

Telomeres Parameters in Cirrhosis

Start date: June 2014
Phase: N/A
Study type: Observational

There are several factors that influence telomere length in patients with cirrhosis, such as metabolic derangements and infectious etiologies, The aim of the study is to compare telomere length and other parameters related to genetic instability in telomere/ telomerase system, in peripheral blood lymphocytes in cirrhosis from different etiologies.

NCT ID: NCT02125071 Completed - Liver Cirrhosis Clinical Trials

Study on the Pharmacokinetic Characteristics of I.V. Hepabig Injection Used for Prevention of Hepatitis B Relapse After Liver Transplantation

LT
Start date: November 2013
Phase: N/A
Study type: Observational

An exploratory clinical trial to evaluate the pharmacokinetic characteristics of I.V. Hepabig injection used for prevention of hepatitis B relapse after liver transplantation.

NCT ID: NCT02124577 Recruiting - Clinical trials for Non-alcoholic Fatty Liver Disease

Development of Kinetic Biomarkers of Liver Fibrosis Measuring NAFLD

Start date: May 2014
Phase:
Study type: Observational [Patient Registry]

This is a small preliminary study conducted to explore new methods for the potential of aiding in diagnosis of liver fibrotic disease as well as predicting disease progression. There will be a total of 4 visits spread out over approximately 8 weeks. You will be asked to drink "heavy water" during most of that time. "Heavy Water" also known as deuterated water, is physically and chemically very similar to ordinary drinking water. It tastes and feels exactly like regular water. It is odorless and has no known harmful effects at the doses given here. Heavy water occurs naturally, and is a minor component of the water we all ingest daily.

NCT ID: NCT02120196 Recruiting - Liver Cirrhosis Clinical Trials

Comparative Study of Rifaximin Versus Norfloxacin in the Secondary Prophylaxis of Spontaneous Bacterial Peritonitis

SBP
Start date: January 2014
Phase: Phase 3
Study type: Interventional

The aim of the study is to compare the effectiveness of rifaximin versus norfloxacin for secondary prevention of spontaneous bacterial peritonitis in patients with liver cirrhosis and ascites.

NCT ID: NCT02119988 Completed - Liver Cirrhosis Clinical Trials

TIPS Combined With Variceal Embolization for the Prevention of Variceal Rebleeding in Patients With Cirrhosis

Start date: June 16, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether TIPS combined with variceal embolization are effective in the prevention of variceal rebleeding in patients with liver cirrhosis.

NCT ID: NCT02085915 Completed - Infection Clinical Trials

Evaluation of the Strip PeriScreen for the Fast Diagnosis of the Spontaneous Infection of the Liquid of Ascites During the Cirrhosis

Per-DRISLA
Start date: March 2014
Phase: N/A
Study type: Interventional

The forecast of the spontaneous infection of the liquid of ascites (ISLA) at the cirrhotic patient is still burdened by a heavy mortality. The fast diagnosis of the ISLA is thus an essential stake to improve the forecast. Investigators would so like to estimate the interest of the strip PeriScreen for the fast diagnosis of the ISLA at cirrhotic patients . Investigators plan to include 670 patients, what would allow to make out a will at least on ascites 2000 on about twenty centers for duration estimated of 12 months.