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Liver Diseases clinical trials

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NCT ID: NCT02938871 Recruiting - Liver Disease Clinical Trials

Effect of Synbiotic on Postoperative Complications After Liver Transplantation

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of synbiotic in patients after liver transplantation and assess the effect of these agents on postoperative infections, antibiotic use, length of hospital stay, mortality and nutritional status.

NCT ID: NCT02938013 Completed - HIV Clinical Trials

deLIVER: Direct Acting Antiviral Effects on the Liver

deLIVER
Start date: January 2017
Phase: Phase 4
Study type: Interventional

Open-label, partially-randomized plasma and liver sampling study to assess hepatitis C virus (HCV) kinetics during treatment with two (Sofosbuvir/Velpatasvir) or three (Sofosbuvir/Velpatasvir/Voxilaprevir) direct acting antivirals (DAAs)

NCT ID: NCT02917408 Completed - Liver Cirrhosis Clinical Trials

Retrospective Study About Primary Biliary Cholangitis During January 2001 to July 2016 at West China Hospital

Start date: September 2016
Phase:
Study type: Observational

Retrospective study of all patients diagnosed with primary biliary cholangitis during January 2001 to July 2016 at West China Hospital by review of medical records. The following variables will be retrospectively studied: age, sex, first symptoms, clinical characteristics, pathology, treatment, stage, complications of cirrhosis, other autoimmune diseases and long-term outcome.

NCT ID: NCT02917382 Recruiting - Liver Disease Clinical Trials

Evolution and Clinical Outcomes in Patients Undergoing Liver Transplantation

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

Liver transplantation (LTx) is the standard treatment used in the final stage of chronic or acute liver failure. The success for the LT depends on many factors. One of the factors related to morbidity and mortality of these patients is malnutrition. Patients on the waiting list for LTx are increased risk of malnutrition and metabolic disorders that may be associated with decreased functional capacity, change in resting energy expenditure cardiac autonomic dysfunction. These conditions may influence the results both before and after transplantation, as the clinical outcome and complications present in the postoperative period. Therefore, this study aims to characterize and relate nutritional status, metabolic, functional and clinical outcomes in the recent postoperative patients undergoing liver transplantation. It is an observational, prospective study based on four evaluations: the first will be conducted while the patient is awaiting transplantation; and after insertion of the graft, patients will be evaluated between the 1nd and 3th postoperative day, between 5 and 7 days and at discharge from hospital. In the late post-transplant, there is the action of immunosuppressive drugs, largely responsible for increased survival, but also on the other hand, are responsible for important nutritional and metabolic disorders. Metabolic complications such as hyperkalemia, hypertension, diabetes mellitus and overweight have been described. Thus, due to the high incidence of these complications, alternative options, such as lowering the dose of immunosuppressive drugs, have been fully explored, particularly as regards association with the viability of the graft. However, few studies have evaluated whether there is change in the incidence of metabolic disorders, cited above, in relation to the different doses of immunosuppressive drugs. Furthermore these metabolic complications will be evaluated in the late post-transplant period.

NCT ID: NCT02908048 Active, not recruiting - Clinical trials for Hepatocellular Carcinoma

Extracellular RNA Markers of Liver Disease and Cancer

Start date: July 2014
Phase:
Study type: Observational [Patient Registry]

The study will examine and evaluate the use of extracellular RNA in blood as markers for the diagnosis of liver disease or cancer, and as markers for prediction of response to treatment or recurrence of cancer after surgery

NCT ID: NCT02901119 Recruiting - Liver Disease Clinical Trials

Effects of Whey Protein Consumption by Patients Waiting for Liver Transplantation

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

Malnutrition is prevalent among chronic liver disease patients. Inadequate ingestion and/or metabolic alterations modify the body composition and biological functions. The purpose of this study is to determine whether whey protein comsumption, due to amino acid profile, digestibility and bioactive compounds may be beneficial for patients waiting for liver transplantation

NCT ID: NCT02877602 Completed - Liver Diseases Clinical Trials

Patient Understanding of LiverMultiScan

Start date: February 2016
Phase: N/A
Study type: Observational

This is a qualitative study to determine which factors affect the patient experience of having a liver MRI, what information patients would like to receive after their MRI, and how patients would like this information communicated to them.

NCT ID: NCT02873663 Active, not recruiting - Alcohol Abuse Clinical Trials

Biomarkers for the Detection of Heavy Alcohol Use in Patients With and Without Liver Disease

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

The investigators will test the validity of biomarkers for the detection of heavy alcohol use in patients with and without liver disease.

NCT ID: NCT02798861 Completed - Liver Disease Clinical Trials

Controlled Attenuation Parameter (CAP) in Liver Allografts

Start date: September 7, 2016
Phase:
Study type: Observational

The primary aim is to determine the accuracy of CAP in the quantification of liver steatosis using liver biopsies as reference. Secondarily, investigators will correlate transient elastography (TE) and CAP results, analyze possible associations between CAP/TE and post-liver transplant (LT) clinical outcomes, and evaluate the change in CAP after LT. The study aims to include as many donors as needed to achieve at least 120 transplanted liver allografts.

NCT ID: NCT02764671 Recruiting - Hepatitis B Clinical Trials

Safety and Immunogenicity of Recombinant Hepatitis B Vaccines in the Neonates

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

The purpose of this study is to further evaluate the immunogenicity and safety of 10μg/0.5ml Recombinant Hepatitis B Vaccines(Saccharomyces Cerevisiae) in the Healthy Neonates.