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Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

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NCT ID: NCT01389115 Recruiting - Liver Cirrhosis Clinical Trials

Fatty Acids Lipidome and Oxidative Stress in Liver Transplantation

Start date: July 2001
Phase: N/A
Study type: Observational

The purpose of this study is to determine lipid metabolism in chronic liver disease in the attempt to find a useful biomarker of liver function and of prognostic value of graft function in those patients who undergo liver transplant. The present study enrolls subjects with liver cirrhosis (with different ethiology), including subjects eligible for a full-size liver transplantation, and healthy controls.

NCT ID: NCT01387061 Completed - Clinical trials for Hepatocellular Carcinoma

Resection for Multiple Hepatocellular Carcinomas (HCC)

Start date: June 2001
Phase: N/A
Study type: Interventional

Surgical resection in patients with multiple hepatocellular carcinomas (HCC) remains controversial. The aim of this study was to investigate the outcome of a consecutive cohort of patients resected for multiple HCC, without macrovascular invasion, in order to identify clinically reliable parameters to select patients for surgery.

NCT ID: NCT01380951 Recruiting - Liver Cirrhosis Clinical Trials

Safety and Efficacy of Telbivudine on Liver Cirrhosis in Patients With Chronic Hepatitis B (CHB)

Start date: May 2011
Phase: Phase 4
Study type: Interventional

Antiviral treatment on Chronic Hepatitis B (CHB) patients with liver cirrhosis is compulsory and effective. Telbivudine, which is superior to lamivudine in the treatment of CHB,is considered to be appropriate for the antiviral treatment on CHB patients with liver cirrhosis.

NCT ID: NCT01379469 Terminated - Liver Cirrhosis Clinical Trials

Carbamazepine in Severe Liver Disease Due to Alpha-1 Antitrypsin Deficiency

CBZ
Start date: January 2012
Phase: Phase 2
Study type: Interventional

The primary objective is to determine if the medication Carbamazepine, can be used as a therapy for patients with severe liver disease due to Alpha-1-Antitrypsin Deficiency .

NCT ID: NCT01370161 Completed - Clinical trials for Decompensated Cirrhosis

Early TIPS With Polytetrafluoroethylene (PTFE) Covered Stents for Acute Variceal Bleeding in Patients With Advanced Cirrhosis

Start date: July 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether early use of transjugular intrahepatic portosystemic shunt (TIPS) with Polytetrafluoroethylene (PTFE) covered stents is able to prolong the survival in patients with advanced cirrhosis and acute variceal bleeding.

NCT ID: NCT01369979 Completed - Liver Cirrhosis Clinical Trials

Hepatic Sugar Metabolism Measured by PET/CT in Patients and Healthy Subjects

Start date: May 2011
Phase: N/A
Study type: Observational

The investigators wish to determine the lumped constant (LC), which is a correction factor necessary for converting measurements of hepatic FDG metabolism (measured by PET) to those of regular glucose in patients with cirrhosis and healthy subjects. Working hypothesis - LC for FDG in liver tissue is not significantly different from unity in healthy subjects - LC for FDG in liver disease is significantly different from LC in healthy liver - Insulin changes the LC for FDG in liver tissue, but not by the same factor in liver disease and healthy subjects.

NCT ID: NCT01361061 Completed - Liver Cirrhosis Clinical Trials

AFP - L3% and DCP as Screening Marker for a Hepatocellular Carcinoma in Patients With Cirrhosis of the Liver

Start date: June 2010
Phase:
Study type: Observational

Hepatocellular carcinoma (HCC) is one of the tumors with a rising incidence worldwide. The aim of this trial is to improve the detection of early HCC nodules in the liver. At the moment screening for HCC in patients with liver cirrhosis is performed by ultrasound and measurement of alpha- fetoprotein (AFP). In this trail the tumor markers AFP- L3 (a subfraction of AFP) and Des-y- carboxyprothromib (DCP) are measured in addition in order to receive information about the course of these markers before the detection of a HCC nodule.

NCT ID: NCT01359462 Completed - Ascites Clinical Trials

Multiple-dose Pharmacokinetics Study of Tolvaptan Tablets in Chinese Patients With Hepatocirrhosis

Start date: April 2009
Phase: Phase 1
Study type: Interventional

For hepatic cirrhosis subjects with ascites or lower extremities, to study Pharmacokinetics, pharmacology, and safety of the drug under fasting condition.

NCT ID: NCT01358123 Recruiting - Liver Cirrhosis Clinical Trials

Value of Von Willebrand Factor in Portal Hypertension

Start date: September 2006
Phase: N/A
Study type: Observational

In patients with liver cirrhosis elevated levels of von Willebrand factor antigen (vWF-Ag) are found frequently but the clinical significance is unclear. vWF-Ag plays an important role in primary haemostasis and development of thrombotic vascular obliteration is discussed as a possible mechanism leading to portal hypertension. Invasive measurement of hepatic venous pressure gradient (HVPG) is the current gold standard for the diagnosis of portal hypertension. The investigators hypothesize that vWF-Ag levels in plasma may correlate with portal pressure and predict clinically significant portal hypertension (CSPH, HVPG >=10mmHg) and its complications.

NCT ID: NCT01355107 Completed - Hepatitis C Clinical Trials

Comparison of Selenium Levels in HCV- Infected Patients at Different Stages of Disease

Start date: April 2011
Phase: N/A
Study type: Observational

The incidence of hepatocellular carcinoma (HCC) is rising worldwide.One important etiology is a chronic inflammation due to hepatitis c (hcv) infection. Over the steps of a chronic inflammation over the stadium of cirrhosis of the liver it is possible that neoplastic nodules appear in the liver which can rise up to a HCC. In the pathogenesis of HCC oxidative stress seems to play an important role and as selenium is a key micronutrient in this process its levels could differ between the different stages of disease in hcv- infected patients. The aim of this trial is to examine these differences.