Clinical Trials Logo

Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

Filter by:

NCT ID: NCT00301509 Completed - Clinical trials for Liver Cirrhosis, Experimental

Antiviral Therapy in Decompensated Hepatitis C Virus (HCV) Cirrhosis

Start date: January 2002
Phase: Phase 2/Phase 3
Study type: Interventional

To evaluate: 1. the impact of combined antiviral therapy (Peginterferon plus ribavirin) on natural history of patients affected with HCV decompensated cirrhosis, after sustained virological response. A controlled study. 2. safety and efficacy of antiviral therapy in this population by using a statistically significally number of patients as controls.

NCT ID: NCT00298714 Completed - Chronic Hepatitis C Clinical Trials

Effects of Losartan on Hepatic Fibrogenesis in Chronic Hepatitis C

Start date: March 2003
Phase: Phase 4
Study type: Interventional

There is evidence on the beneficial effects of the administration of angiotensin II type 1 (AT1) receptors antagonists on liver fibrosis in hepatic stellate cells, experimental models of liver fibrosis in rodents and limited information in chronic hepatitis C with mild fibrosis. The purpose of this study is to investigate the effect of long-term administration of oral Losartan, an AT1 receptor antagonist, on liver fibrogenesis in patients with chronic hepatitis C and fibrosis F2-F3 (METAVIR score).

NCT ID: NCT00296244 Completed - Liver Cirrhosis Clinical Trials

Steroid Free Immunosuppression in Liver Transplantation

Start date: February 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether steroid-related complications can be avoided by using steroid-free immuno-suppressive drug regimen after liver transplantation.

NCT ID: NCT00287664 Suspended - Cirrhosis Clinical Trials

Treatment of Hepatorenal Syndrome With Terlipressin Plus Albumin vs Albumin

Start date: February 2002
Phase: Phase 4
Study type: Interventional

Hepatorenal syndrome is a common complication of cirrhotic patients. The prognosis of patients with HRS is very poor. It have been demonstrated that vasoconstrictors agents (Terlipressin) plus albumin are effective in the reversal of the treatment. However, previous studies are pilot studies and they are not able to give information about an improvement in survival. This comparative randomized study was delineated to test the efficacy of terlipressin on survival.

NCT ID: NCT00287235 Completed - Liver Cirrhosis Clinical Trials

Efficacy of Albumin Dialysis to Treat Patients With Hepatic Encephalopathy Using The Molecular Adsorbent Recirculating System (MARS)

Start date: September 2000
Phase: N/A
Study type: Interventional

The primary objective of the study was to compare the efficacy, safety and tolerability of Extracorporeal Albumin Dialysis (ECAD) using the Molecular Adsorbent Recirculating System (MARS®) device in improving severe HE by 2 grades compared to Standard Medical Therapy (SMT) in patients with chronic End Stage Liver Disease (ESLD) during a 5 day study period.

NCT ID: NCT00281502 Recruiting - Hepatitis C Clinical Trials

The Role of Bacterial Overgrowth and Delayed Intestinal Transit in Hepatic Encephalopathy

Start date: December 2005
Phase: Phase 2
Study type: Interventional

The study will be conducted in two phases. Phase A will evaluate the contribution of bacterial overgrowth and colonic inertia to development of Hepatic Encephalopathy (HE)in 50 ambulatory subjects with HE and hepatitis C cirrhosis. This phase will include a Screening and Evaluation Visit. Phase B will evaluate the effect of rifaximin on bacterial outgrowth and severity of HE in 20 of the subjects enrolled in Phase A who have a somewhat greater degree of encephalopathy. The purpose of this study is to evaluate the following: 1. the relationship between bacterial overgrowth and the presence and severity of HE in patients with hepatitis C cirrhosis; 2. the effectiveness and tolerability of rifaximin relative to placebo in treatment of HE associated with hepatitis C cirrhosis; 3. the relationship between bacterial overgrowth and the presence and severity of HE before and after rifaximin treatment.

NCT ID: NCT00275652 Completed - Hepatitis B Clinical Trials

A Comparison of the Drug Telbivudine (LdT) and Lamivudine in Adults With Decompensated Chronic Hepatitis B and Evidence of Cirrhosis.

Start date: June 2004
Phase: Phase 3
Study type: Interventional

This trial is being done to see if the investigational drug, LdT (Telbivudine), is safe and effective in the treatment of hepatitis B infection. In addition to this, we will be looking at the comparison of the effects (good and bad) of LdT and lamivudine.

NCT ID: NCT00273247 Completed - Clinical trials for Hepatocellular Carcinoma

Treatment With IFN After Curative Resection of HCC in HCV-Related Cirrhosis

Start date: June 1998
Phase: Phase 3
Study type: Interventional

We conducted a randomized controlled trial of adjuvant interferon (IFN) therapy in patients with hepatitis-C virus (HCV)-related cirrhosis who underwent curative resection of hepatocellular carcinoma (HCC) to investigate whether IFN could reduce or delay the incidence of recurrent tumor (secondary/tertiary prevention of HCC). Patients were randomly assigned to treatment with IFN (3MU thrice/wk /48 weeks) vs. no treatment after curative resection of HCC(control group)

NCT ID: NCT00252642 Completed - Hepatitis C Clinical Trials

Peginterferon Alpha-2a Maintenance Therapy for Portal Hypertension in Patients With Hepatitis C

Start date: November 2005
Phase: N/A
Study type: Interventional

The primary purpose of this study is to determine if peginterferon alpha-2a maintenance therapy (90 mcg/week) will lower portal pressure in patients with hepatitis C virus infections and advanced fibrosis or cirrhosis.

NCT ID: NCT00250315 Completed - Cirrhosis Clinical Trials

DOCICAR: Cardiac Dysfunction in Cirrhosis

Start date: November 2005
Phase: Phase 3
Study type: Observational

Patients with cirrhosis have a altered cardiac response to stress. This study evaluate the cardiac response by MRI during dobutamine stress. Hypothesis: impared increase in cardiac output, cardiac index, ejection fraction.