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Cirrhosis clinical trials

View clinical trials related to Cirrhosis.

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NCT ID: NCT02319200 Terminated - Clinical trials for Hepatocellular Carcinoma

Primary Prevention Hepatocellular Carcinoma by Metformin

METFOVIR
Start date: June 2015
Phase: Phase 3
Study type: Interventional

Metformin treatment during 36 months could be associated with decreased risk of HCC occurrence and liver related death in patients with compensated HCV cirrhosis and insulinoresistance. This study is an ancillary of the observational study from the CIRVIR cohort in which more than 1200 patients with compensated HCV cirrhosis are currently included. participating centers : 26

NCT ID: NCT02313896 Terminated - Cirrhosis Clinical Trials

Cirrhosis Readmission Telehealth Project

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

This is a 2 year research study to study if post discharge phone calls can help lengthen time to hospital readmissions for patients with encephalopathy.

NCT ID: NCT02310165 Completed - Cirrhosis Clinical Trials

Insertion Technique in Large Volume Paracentesis

Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two different methods that are used for inserting the needle during paracentesis. One method is called the "coaxial insertion technique" and the other is called the "z-tract technique". Researchers would like to see which method is better and leads to less problems like oozing from the needle insertion site and pain during the procedure. Both methods are approved and currently used methods for doing a paracentesis at the University of Virginia. Which method is used generally depends on physician preference. There have been no studies done to date that compare these two methods for needle insertion.

NCT ID: NCT02304159 Completed - Hepatitis C Clinical Trials

Study to Evaluate the Safety and Efficacy of Daclatasvir/Sofosbuvir/Ribavirin for 16 Versus 24 Weeks for HCV Genotype 3 Cirrhotics

Start date: January 2015
Phase: Phase 4
Study type: Interventional

This is a randomized, open label, single center safety and efficacy study. At least 40 cirrhotic subjects with HCV genotype 3 will receive standard of care treatment of sofosbuvir and ribavirin (SOF/RBV) as well as 60 mg daily of Daclatasvir (investigational product). Subjects will be randomized in a 1:1 to receive either: - Group A: 16 weeks of DCV/SOF/RBV - Group B: 24 weeks of DCV/SOF/RBV Subjects will return to the study center at various time points throughout the 16 or 24 weeks of treatment in addition to 12 weeks post taking last dose of study drug to monitor safety and efficacy. These visits will be according to standard of care.

NCT ID: NCT02298868 Completed - Cirrhosis Clinical Trials

Safety and Efficacy of Baclofen for Treatment of Muscle Spasms in Patients With Cirrhosis: A Pilot Study

Start date: October 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of the medication Baclofen for treatment of muscle cramps in patients with cirrhosis.

NCT ID: NCT02275585 Withdrawn - Cirrhosis Clinical Trials

Portal Vein Thrombosis in Cirrhosis

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

This study evaluates the supervivence of cirrhotic patients that develop portal vein thrombosis in comparison to cirrhotic patients that do not develop portal vein thrombosis.

NCT ID: NCT02273362 Completed - Clinical trials for Hepatocellular Carcinoma

Erlotinib Hydrochloride in Preventing Liver Cancer in Patients With Cirrhosis of the Liver

Start date: November 24, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This pilot phase I/II trial studies the best dose of erlotinib hydrochloride and to see how well it works in preventing liver cancer in patients with scarring (cirrhosis) of the liver. Erlotinib hydrochloride may help to inhibit the development of fibrous tissue and prevent liver cancer from forming in patients with cirrhosis of the liver.

NCT ID: NCT02272504 Active, not recruiting - Cirrhosis Clinical Trials

A Protocol of the Canadian Prospective Study for Hepatocellular Carcinoma Surveillance Using Biomarkers

Start date: August 2014
Phase:
Study type: Observational

The objective of this study is to evaluate the clinical effectiveness of biomarkers, alpha-fetoprotein (AFP), Lens culinaris agglutinin-reactive fraction of AFP (AFP-L3), and des-gamma-carboxy prothrombin (DCP), for surveillance program patients whose hepatocellular carcinoma (HCC) development may be potentially missed by ultrasound (US). This study expects to demonstrate that addition of biomarkers will increase the detection rate by at least 10%.

NCT ID: NCT02271295 Suspended - Cirrhosis Clinical Trials

Impact on Morbidity and Mortality of Prophylactic Dosing of Low Molecular Heparin in Child-Pugh B Cirrhotic Patients

Childbenox
Start date: July 27, 2015
Phase: Phase 3
Study type: Interventional

Thrombosis occurring in the small intrahepatic, as well as in the large vessels is involved in the progression of cirrhosis. Anticoagulation could reduce morbidity and mortality in cirrhotic patients

NCT ID: NCT02267421 Completed - Cirrhosis Clinical Trials

Effects of Home Based Exercise Therapy in Early Cirrhosis

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

Individuals with Cirrhosis have been shown to have a low aerobic capacity. While supervised exercise training has been shown to be an effective intervention to remedy this, there is currently no data on home based exercise interventions in this population. This study will evaluate the effects of a home based exercise program on the aerobic capacity of enrolled early stage liver cirrhosis patients, as well as changes in quality of life, thigh muscle thickness, and thigh muscle oxygen consumption.