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Hepatitis A clinical trials

View clinical trials related to Hepatitis A.

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NCT ID: NCT02120274 Terminated - Hepatitis C Clinical Trials

Vitamin D and Vitamin B12 Supplementation With Pegylated Interferon-Alfa Plus Ribavirin for Treating Chronic Hepatitis C

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of the supplementation of vitamins D and B12 in combination with Pegylated Interferon-Alfa and Ribavirin in the treatment of genotype 1 chronic hepatitis C, who do not qualify to receive protease inhibitor in Brazil.

NCT ID: NCT02065336 Terminated - Clinical trials for Hepatitis B, Chronic

A Multicenter Study to Determine the Depth and Duration of Hepatitis B Surface Antigen (HBsAg) Reduction After Single or Multiple Doses of ARC-520, in Combination With Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether ARC-520 in combination with entecavir is effective in the treatment of patients with chronic HBV Infection.

NCT ID: NCT02058108 Terminated - Chronic Hepatitis B Clinical Trials

Study of Efficacy and Safety, Tolerability and Pharmacokinetics of Telbivudine in Children and Adolescents With Compensated Chronic Hepatitis B Virus Infection

Start date: October 31, 2014
Phase: Phase 3
Study type: Interventional

The purpose of the study was to assess the efficacy and safety of telbivudine at a dose of 20 mg/kg up to a maximum of 600 mg q.d. in compensated pediatric HBeAg-positive and negative CHB patients aged 2 to <18 years with the indication of antiviral CHB treatment. This study was part of the commitments of the pediatric development plan for telbivudine in Europe and US.

NCT ID: NCT02056054 Terminated - Clinical trials for De Novo Autoimmune Hepatitis

De Novo Autoimmune Hepatitis in Pediatric Liver Transplantation

Start date: September 9, 2013
Phase:
Study type: Observational

The purpose of this study is to provide insights into the cause, development and effects of de novo autoimmune hepatitis so that prevention and treatment strategies can be developed in order to reduce post-liver transplant morbidity, the frequency of liver allograft loss and the need for re-transplantation.

NCT ID: NCT02039219 Terminated - Alcoholic Hepatitis Clinical Trials

Trial of Obeticholic Acid in Patients With Moderately Severe Alcoholic Hepatitis (AH)

TREAT
Start date: November 3, 2014
Phase: Phase 2
Study type: Interventional

The main purpose of this study is to test the effectiveness of Obeticholic Acid when used in patients with moderately severe alcoholic hepatitis. The researchers suspect that individuals with alcoholic hepatitis have certain abnormalities in how their body handles bile acids (a product made by the liver on a daily basis) produced by the liver. Obeticholic acid has been shown to affect bile acid abnormalities and thus it is possible that obeticholic acid may improve liver condition in individuals with alcoholic hepatitis.

NCT ID: NCT01951209 Terminated - Liver Cirrhosis Clinical Trials

Pilot Study Of The Effect Of Rifaximin On B-Cell Dysregulation In Cirrhosis

Start date: November 17, 2016
Phase: N/A
Study type: Interventional

Hepatitis C is the leading cause of chronic liver disease and cirrhosis in United States veterans. Cirrhosis is associated with impaired antibody responses and increased risk of bacterial infections. We have recently identified that cirrhosis is associated with abnormalities of memory B-cells, cells that make antibodies and help protect against bacterial infections. We have identified that chemicals associated with gut bacteria might play a role in causing these B-cell abnormalities. It is well known that gut bacteria have increased access to the blood in individuals with cirrhosis, a process called bacterial translocation. We hypothesize that reducing bacteria counts in the gut by using poorly-absorbed antibiotics (also known as selective gut decontamination) will partially reverse losses of memory B-cells in cirrhosis by reducing bacterial translocation.

NCT ID: NCT01922895 Terminated - Clinical trials for Acute Alcoholic Hepatitis

Novel Therapies in Moderately Severe Acute Alcoholic Hepatitis

NTAH-Mod
Start date: August 1, 2013
Phase: N/A
Study type: Interventional

This study is being done to find out whether a diet supplemented with a probiotic nutrient can improve alcoholic hepatitis and gut complications compared to routine standard care.

NCT ID: NCT01890083 Terminated - Clinical trials for Major Depressive Disorder

A Health Intervention to Prevent Depression Hepatitis C Patients

Start date: June 2013
Phase: Phase 2/Phase 3
Study type: Interventional

Interferon-alpha (IFN-α) is an efficacious treatment for Hepatitis C (HPC); however, IFN-α treatment results in a significant increase in depressive symptoms. The aim of this project is to compare two health interventions (exercise vs. health education) to prevent depression in HPC patients receiving IFN-α. Participants will be recruited from the Clinical Center for Liver Diseases at UT-Southwestern and randomized to 26 weeks of either: aerobic exercise or a health education control group.

NCT ID: NCT01886300 Terminated - Clinical trials for Hepatitis B, Chronic

An Observational Study of Pegasys (Peginterferon Alfa-2a) in Patients With HBeAg-Positive Chronic Hepatitis B in Vietnam

Start date: September 2012
Phase: N/A
Study type: Observational

This prospective, multicenter, observational study will evaluate the sustained response in patients with HBeAg positive chronic hepatitis B who are treated with Pegasys according to standard of care and in line with the current local labeling in routine clinical practice in Vietnam. Eligible patients will be followed for the duration of their treatment and for up to 2 years thereafter.

NCT ID: NCT01861444 Terminated - Clinical trials for Hepatitis D, Chronic

An Observational Study on the Prevalence of Chronic Hepatitis D in Romania and the Efficacy of Treatment With Pegasys (Peginterferon Alfa-2a)

Start date: March 2011
Phase: N/A
Study type: Observational

This prospective, multicenter, observational study will assess the prevalence of chronic hepatitis D in patients with chronic hepatitis B in Romania and evaluate the efficacy of Pegasys (peginterferon alfa-2a) in patients with chronic hepatitis D. Eligible patients treated with Pegasys according to current medical practice will be followed until 24 weeks after the end of treatment.