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Hepatitis, Alcoholic clinical trials

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NCT ID: NCT03452540 Terminated - Clinical trials for Severe Acute Decompensated Alcoholic Hepatitis

Efficacy and Safety of Orally Administered DS102 in Patients With Acute Alcoholic Hepatitis

Start date: November 28, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this randomised, double-blind, placebo-controlled, phase II study is to assess the efficacy and safety of orally administered DS102 in adult patients with acute decompensated alcoholic hepatitis

NCT ID: NCT02612428 Terminated - Clinical trials for Acute Alcoholic Hepatitis

Randomized, Open-Label, Multicenter, Controlled, Pivotal Study to Assess Safety and Efficacy of ELAD in Subjects w/ AILD

Start date: January 2016
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to evaluate safety and efficacy of ELAD with respect to overall survival of subjects with a clinical diagnosis of alcohol-induced liver decompensation (AILD) through at least Study Day 91. The secondary objective is to evaluate the proportion of survivors at Study Day 91 using a chi-squared test.

NCT ID: NCT02442180 Terminated - Alcoholic Hepatitis Clinical Trials

Efficacy and Safety of G-CSF in Patients With Severe Alcoholic Hepatitis With Null or Partial Response to Steroid

GraCiAH
Start date: July 2015
Phase: Phase 3
Study type: Interventional

Steroid is the treatment of choice in patients with severe alcoholic hepatitis. However, null- or partial responder of steroid treatment is recommended to consider liver transplantation. The yearly demand for liver transplants far exceeds the supply of available organs and alcoholic liver disease has been a controversial indication for transplantation. Granulocyte-Colony Stimulating Factor (G-CSF) has been reported to have effect of proliferation of hepatic progenitors in alcoholic steatohepatitis. The aim of this study is to investigate the efficacy of G-CSF in patients with severe alcoholic hepatitis with null or partial response to steroid.

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: NCT01937130 Terminated - Liver Cirrhosis Clinical Trials

Pharmacokinetic and Pharmacodynamic Study of IDN-6556 in ACLF

Start date: September 2013
Phase: Phase 2
Study type: Interventional

The study will evaluate the pharmacokinetics, pharmacodynamics, safety and preliminary efficacy of IDN-6556 in subjects with cirrhosis of the liver who are hospitalized for more than 24 hours due to acute deterioration of liver function.

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: NCT01912404 Terminated - Alcoholic Hepatitis Clinical Trials

Study of IDN-6556 in Patients With Severe AH and Contradictions to Steroid Therapy

AH
Start date: July 2013
Phase: Phase 2
Study type: Interventional

The main purpose of the study is to test if taking a study drug called emricasan (also known as IDN-6556 and PF-03491390) will affect overall patient survival after one month of treatment.

NCT ID: NCT01829347 Terminated - Clinical trials for Severe Acute Alcoholic Hepatitis

To Assess Safety/Efficacy of ELAD in Subjects w/ Severe Acute Alcoholic Hepatitis (sAAH) and Lille Score Failure

Start date: April 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if treatment with the ELAD System is safe and effective in subjects with severe acute alcoholic hepatitis and Lille score failures (Lille score >0.45).

NCT ID: NCT00205049 Terminated - Clinical trials for Hepatitis, Alcoholic

Pentoxifylline for Acute Alcoholic Hepatitis (AAH)

Start date: March 2005
Phase: Phase 1
Study type: Interventional

The goal of this study is to demonstrate the effectiveness of pentoxifylline compared to placebo in AAH while studying putative mechanisms that are plausible and testable. The main hypothesis is that pentoxifylline reduces the 90-day mortality of AAH.