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Chronic Liver Disease clinical trials

View clinical trials related to Chronic Liver Disease.

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NCT ID: NCT02359266 Completed - Depression Clinical Trials

Vitamin D Improves Depression in Liver Patients

CLDVitD
Start date: December 2011
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of vitamin D replacement therapy in reducing depressive symptoms in patients with chronic liver disease and vitamin D deficiency. Patients with normal vitamin D levels will be monitored as controls, and they will not receive any intervention.

NCT ID: NCT02347319 Completed - Clinical trials for Chronic Liver Disease

To Evaluate the Efficacy of DDB/Garlic Oil in Patients With Elevated Transaminase Chronic Liver Disease

Start date: April 2012
Phase: Phase 4
Study type: Interventional

Purpose - To evaluate the efficacy of Biphenyl dimethyl dicarboxylate(DDB)/Garlic Oil in patients with elevated transaminase chronic liver disease.

NCT ID: NCT02294292 Completed - Clinical trials for Chronic Liver Disease

Therapeutic Approach to Diastolic Dysfunction in Chronic Liver Disease Patients and Its Impact on Morbidity and Mortality

Start date: July 1, 2014
Phase: N/A
Study type: Interventional

Cirrhotic cardiomyopathy is defined as a chronic cardiac dysfunction in patients with cirrhosis. It is suspected that this specific cardiac dysfunction contributes to the onset of complications in liver disease. The purpose of this prospective, randomized controlled trial is to determine whether carvedilol can revert cardiac dysfunction i.e. left ventricular diastolic dysfunction secondary to cirrhosis, and prevent complications (renal dysfunction, worsening cardiac function, and mortality).

NCT ID: NCT02184000 Recruiting - Cirrhosis Clinical Trials

The Role of Strain Elastography in Staging Liver Fibrosis

SELF
Start date: March 2014
Phase: N/A
Study type: Observational

AIM: To evaluate the role of Strain Elastography in the assessment of liver fibrosis in chronic hepatopathy

NCT ID: NCT02086708 Recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

Ultrasound Method to Measure Fibrosis of the Liver in Children

Start date: June 2010
Phase: N/A
Study type: Interventional

HYPOTHESIS: The investigators hypothesize that sonoelastography (SE) provide accurate quantitative measurements that can be used to stage liver fibrosis in pediatric patients with chronic liver disease. Specific Aims: 1. To measure liver stiffness with sonoelastography in adults with suspect diffuse liver disease who will undergo nonfocal liver biopsy as part of their routine clinical care. 2. To assess the sensitivity and specificity of sonoelastography for the detection and staging of liver fibrosis. 3. To obtain sonoelastography values of the liver in healthy children (control subjects).

NCT ID: NCT02084160 Completed - Clinical trials for Chronic Liver Disease

Prediction Value of the BreathID 13C-Methacetin Breath Test for Hepatic Decompensation

Start date: March 2014
Phase:
Study type: Observational

The objectives of this study are: - To evaluate the ability of the Methacetin Breath Test (MBT) to detect hepatic decompensation events - To evaluate the relationship between liver Biopsy and clinical outcome and show that the MBT has a better predictive ability of clinical outcome than liver biopsy. - To evaluate the ability of the MBT to predict each of the individual liver related complications.

NCT ID: NCT02060565 Recruiting - Clinical trials for Chronic Liver Disease

Prognosis Value of Non-invasive Methods for the Diagnosis of Chronic Liver Disease

PVNIM
Start date: February 2014
Phase:
Study type: Observational

The aim of this retrospective and prospective study is to evaluate the 20-year prognosis value of non-invasive methods for the diagnosis of chronic liver disease for predicting survival and complications of cirrhosis.

NCT ID: NCT02037867 Recruiting - Obesity Clinical Trials

Nottingham Community Liver Biomarkers Cohort

Start date: May 2013
Phase:
Study type: Observational [Patient Registry]

Deaths due to advanced liver scarring (liver cirrhosis) continue to increase, and liver disease is now the 3rd leading cause of premature death in the United Kingdom. The majority of liver disease is lifestyle related (alcohol, obesity and associated type 2 diabetes, injecting drug use) and therefore reversible if caught at a precirrhosis stage. However, current liver function blood tests are poor inadequate, and subsequently a large burden of liver disease is currently missed. A variety of noninvasive liver biomarkers (blood and imaging tests) have been developed which identify liver disease accurately at earlier stages of scarring. The identification of liver disease in the community, where previous studies have discovered a large burden of previously unidentified but significant liver disease, is therefore a feasible place to develop new liver disease investigation pathways using these noninvasive markers. In collaboration with the Department of Health, Nottingham University Hospitals have commenced a pilot community liver disease pathway in two General Practices in Nottingham in February 2012. Patients with liver risk factors (hazardous alcohol use, obesity or type 2 diabetes)are invited to take part in the pathway. Patients undergo a simple blood test (AST:ALT ratio and BARD score), with a high test result requiring referral for a liver stiffness scan (Fibroscan)which is performed in the community setting. High threshold scan values are reviewed by a consultant liver specialist in a community liver clinic. Preliminary findings show that the pathway accurately identifies patients with early liver scarring and previously unidentified significant liver disease. The participating General Practitioners have also noted a striking number of patients finally engaging in important lifestyle changes following pathway implementation. A second phase of the pilot pathway, in 2 Inner City General Practices with a total practice population of c.14,000 patients commenced in June 2013. We have subsequently designed this cohort study, where pilot participants will be consented for follow up over a long period. We will assess future liver-related and cardiovascular events (including death), and perform qualitative patient interviews to assess the reasons for and persistence of lifestyle changes after liver disease investigation. We hypothesize that stratification of liver disease in the community will unearth a significant amount of previously undetected but significant chronic liver disease. Moreover, we will evaluate whether stratification of liver disease using these tests predicts future liver and cardiovascular disease and death, and whether stratification has an impact on patient's future lifestyle choices.

NCT ID: NCT01948687 Recruiting - Cirrhosis Clinical Trials

Real Time Elastography in Liver Fibrosis

RT-ELASTO
Start date: August 2013
Phase: N/A
Study type: Observational

AIM To evaluate the role of real time elastography (ARFI and Hitachi elastography) in noninvasive diagnosis of liver fibrosis in patients with chronic hepatitis

NCT ID: NCT01944878 Completed - Cirrhosis Clinical Trials

The Association With Peptic Ulcer Disease and Hepatic Vein Pressure Gradient

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

The aim of this study is to assess the role of portal hypertension of peptic ulcer disease in liver cirrhosis and chronic hepatitis.