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Cirrhosis clinical trials

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NCT ID: NCT04940416 Terminated - Cirrhosis Clinical Trials

Eye Movement Testing for Diagnosing Encephalopathy in Patients With Liver Disease

Start date: August 31, 2017
Phase:
Study type: Observational

This study involves utilizing a noninvasive computer application (Neurofit) that performs oculometric assessment of dynamic visual processing in patients with liver cirrhosis to see if the presence of advance liver disease influences eye movement metrics.

NCT ID: NCT04509336 Terminated - Cirrhosis Clinical Trials

Orphenadrine Versus Baclofen in Treatment of Muscle Cramps in Cirrhotic Patients

Start date: August 20, 2020
Phase: N/A
Study type: Interventional

Muscle cramps are commonly affects patients with cirrhosis. It adversely influences the quality of life of cirrhotic patients. Treatment of muscle cramps still challenging owing to the diversity of the responsible pathophysiological mechanisms.The effectiveness of baclofen and orphenadrine in controlling muscle cramps in cirrhotic patients has been presented in recent randomised controlled clinical trials;however, the comparative efficacy and safety between these two therapeutic options has not been previously investigated.

NCT ID: NCT04264754 Terminated - Clinical trials for Hepatocellular Carcinoma

Characterization of Methylation Patterns in Hepatocellular Carcinoma

Start date: February 13, 2018
Phase:
Study type: Observational

This study is being performed as part of the development process of the Liver EpiCheck test which includes the identification of different methylation profiles in HCC (hepatocellular carcinoma) patients compare to cancer free control in blood samples

NCT ID: NCT03827200 Terminated - Cirrhosis Clinical Trials

A Study Evaluating the Utility of Ambrisentan in Lowering Portal Pressure in Patients With Liver Cirrhosis

Start date: April 11, 2019
Phase: Phase 2
Study type: Interventional

Endothelin is a human hormone which has been associated with increased portal pressure in patients with liver cirrhosis (also called portal hypertension). Ambrisentan blocks the effects of endothelin. The purpose of this study is to evaluate the effect of ambrisentan on portal pressure and renal function in patients with advanced liver cirrhosis and with portal hypertension. In this study, portal pressure will be determined at multiple times with the aid of a catheter inserted into the body of the patient. The effect of ambrisentan on the function of the kidney will also be investigated. This study will also evaluate the concentrations of ambrisentan in blood in patients with liver cirrhosis.

NCT ID: NCT03534141 Terminated - Clinical trials for Hepatocellular Carcinoma

Mild Hypothermia and Acute Kidney Injury in Liver Transplantation

MHALT
Start date: July 7, 2018
Phase: N/A
Study type: Interventional

Acute kidney injury (AKI), or worsening kidney function, is a common complication after liver transplantation (20-90% in published studies). Patients who experience AKI after liver transplantation have higher mortality, increased graft loss, longer hospital and intensive care unit stays, and more progression to chronic kidney disease compared with those who do not. In this study, half of the participants will have their body temperature cooled to slightly lower than normal (mild hypothermia) for a portion of the liver transplant operation, while the other half will have their body temperature maintained at normal. The study will evaluate if mild hypothermia protects from AKI during liver transplantation.

NCT ID: NCT03447730 Terminated - Cirrhosis Clinical Trials

Safety, Tolerability and Pharmacodynamics of SYNB1020

Start date: March 19, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This Phase 1b/2a, randomized, double-blind, placebo-controlled study was designed to evaluate the safety, tolerability, and pharmacodynamics of SYNB1020 in hepatic insufficiency and cirrhosis patients with hyperammonemia, with dosing of the investigational medicinal product (IMP) administered in an inpatient unit and subsequent outpatient follow-up for SYNB1020 clearance in two study parts.

NCT ID: NCT03027635 Terminated - Cirrhosis Clinical Trials

PEriToneal Catheter Versus Repeated Paracentesis for Ascites in Cirrhosis

PETRA
Start date: January 20, 2017
Phase: N/A
Study type: Interventional

Insertion of a tunnelated peritoneal catheter (PleurX) allows repeated intermittent small volume fluid drainage at home. The treatment may improve the management of ascites and have a beneficial effect on the quality of life. This study aims to evaluate the beneficial and harmful effects of the peritoneal catheter (PleurX) versus repeated large volume paracentesis for patients with cirrhosis and diuretic resistant ascites. The trial is an investigator initiated, randomised, single blind, parallel arm, controlled trial. Tunnelated peritoneal (PleurX) catheter versus large volume paracentesis. All patients will receive ciprofloxacin to prevent spontaneous bacterial peritonitis. We will include 32 adult patients with cirrhosis Duration of trial 18 months. The total duration of follow up is six months. The primary outcome is paracentesis free survival.

NCT ID: NCT02457988 Terminated - Cirrhosis Clinical Trials

The Cirrhosis Outpatient Optimization, Readmission & Safety Study

Vivify
Start date: April 2015
Phase: Early Phase 1
Study type: Interventional

A prospective series comparing care incorporating home monitoring and liver care coordination to conventional care for patients with cirrhosis.

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.