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Liver Cirrhosis clinical trials

View clinical trials related to Liver Cirrhosis.

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NCT ID: NCT01002001 Enrolling by invitation - Liver Cirrhosis Clinical Trials

Sleep Disorders Pre and Post Liver Transplantation

Start date: October 2009
Phase: N/A
Study type: Observational

Sleep disturbance and sexual dysfunction are common complaints of patients with cirrhosis . The term sleep disturbance describes insomnia, poor quality sleep, circadian rhythm disorders and obstructive sleep apnea and is associated with reduced health-related quality of life (HRQoL) score indices. Sleep and sexual disorders have only been formally evaluated in small studies in these patients and to date, no studies have objectively assessed these patients. In addition, no studies have been performed in these patients after liver transplantation. The investigators' hypothesis is that sleep and sexual disturbance is commonly seen in patients with advanced cirrhosis and improves after liver transplantation. However, despite this, HRQoL remain impaired because of residual sleep disturbance.This study will be unique in providing cross-sectional follow-up of patients with cirrhosis at baseline and after liver transplantation (> 6 months).

NCT ID: NCT00999167 Completed - Cirrhosis Clinical Trials

A Study of Safety and Efficacy of HPN-100 in Subjects With Cirrhosis and Episodic Hepatic Encephalopathy

HALT-HE
Start date: December 2009
Phase: Phase 2
Study type: Interventional

This is a phase 2 study of HPN-100 in subjects with hepatic encephalopathy (HE) consisting of an open label safety lead-in (Part A), followed by randomized, double-blind, placebo-controlled treatment (Part B).

NCT ID: NCT00993941 Active, not recruiting - Liver Cirrhosis Clinical Trials

Bone Mesenchymal Stem Cell (BMSC) Transplantation in Liver Cirrhosis Via Portal Vein

Start date: October 2009
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the therapeutic efficacy of autologous bone marrow mesenchymal stem cells (BMSCs) transplantation via portal vein in patients with early and middle stage of liver cirrhosis on the basis of HBV infection. The evaluation of the efficacy includes the level of serum alanine aminotransferase (ALT), aspartate aminotransferase(AST), total bilirubin (TB),prothrombin time (PT), albumin (ALB), prealbumin(PA), precollagenⅢ(PCⅢ), collagenⅣ(Ⅳ-C), laminin(LN), hyaluronidase(HN), liver histological improvement before and 1 week to 1 year after transplantation. Child-Pugh scores and clinical symptoms were also observed simultaneously.

NCT ID: NCT00978978 Not yet recruiting - Liver Cirrhosis Clinical Trials

Propofol Versus Midazolam and Fentanyl for Diagnostic and Screening Colonoscopy in Patients With Advanced Liver Disease

Start date: October 2009
Phase: N/A
Study type: Interventional

Prospective, randomized-controlled trial (RCT) comparing the use of Propofol and traditional sedation (Midazolam and Fentanyl) for diagnostic and screening endoscopies in patients with liver diseases. The investigators' working hypothesis is that the use of propofol will be translated in a shorter recovery and discharge times with a higher patient satisfaction and a decrease in general complications in the context of patients with advanced liver disease.

NCT ID: NCT00976287 Unknown status - Liver Cirrhosis Clinical Trials

Autologous Bone Marrow Mesenchymal Stem Cells Transplantation Via Hepatic Artery in Patients With Liver Cirrhosis

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the efficacy of autologous bone marrow mesenchymal stem cells (MSCs) transplantation via hepatic artery in the treatment of liver cirrhosis. Liver function was monitored by serum examination. The levels of serum alanine aminotransferase (ALT), total bilirubin (TB), prothrombin time (PT) and albumin (ALB) were examined at pre-transplantation, and 3 days to 2 years post-transplantation. Child-Pugh scores and clinical symptoms were also observed simultaneously.

NCT ID: NCT00968695 Completed - Cirrhosis Clinical Trials

Effects of Long Term Albumin 20% Administration in Patients With Cirrhosis and Ascites.

Start date: July 2009
Phase: Phase 4
Study type: Interventional

Effects of long term albumin administration on the cardiocirculatory and renal function and hepatic hemodynamics in patients with advanced cirrhosis and ascites.

NCT ID: NCT00965900 Recruiting - Cirrhosis Clinical Trials

Endoscopic Band Ligation (EBL) Versus Propranolol for Primary Prophylaxis of Variceal Bleeding

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

This study is performed to compare the efficacy and safety of EBL, propranolol, and EBL combined with propranolol in patients with medium or large varices.

NCT ID: NCT00965744 Completed - Liver Cirrhosis Clinical Trials

A Clinical Trial of the Vessel Sealing System (LigaSure) in Azygoportal Disconnection and Splenectomy in Patients With Portal Hypertension

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

The aim of this trial was to verify the efficiency of a new surgical device (the LigaSure vessels sealing system) in esophagogastric decongestion and splenectomy in patients with portal hypertension.

NCT ID: NCT00956098 Completed - Liver Cirrhosis Clinical Trials

Efficacy and Safety of Oltipraz in the Patients With Liver Fibrosis and Cirrhosis

Start date: February 2006
Phase: Phase 2
Study type: Interventional

This study investigated the effectiveness and safety of oltipraz therapy in treating patients with cirrhosis induced by chronic hepatitis type B or C.

NCT ID: NCT00943176 Completed - Fatigue Clinical Trials

Modafinil in the Treatment of Fatigue in Patients With Primary Biliary Cirrhosis (PBC)

PBC
Start date: June 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the use of modafinil in the treatment of fatigue in patients with Primary Biliary Cirrhosis. The general aim of the study is to identify a safe and effective therapy for fatigue in patients with primary biliary cirrhosis.