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Hepatic Encephalopathy clinical trials

View clinical trials related to Hepatic Encephalopathy.

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NCT ID: NCT02255617 Completed - Clinical trials for Hepatic Encephalopathy

Fecal Microbiota Transplantation (FMT) in the Management of Hepatic Encephalopathy (HE): a Pilot Study

Start date: July 23, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if FMT can reverse Hepatic Encephlopathy (HE) in cirrhotic patients who continue to have breakthrough episodes of HE despite maintenance therapy with lactulose and/or rifaximin or metronidazole.

NCT ID: NCT02173132 Completed - Work Ability Clinical Trials

Acetyl-L-Carnitine Reduces Perceived Work Stress and Improves Work Ability and Work Performance in Hepatic Encephalopathy

Start date: April 2010
Phase: Phase 3
Study type: Interventional

This study evaluated the effects of acetyl-L-carnitine treatment on Perceived Work Stress, Work Ability and Work Performance in subjects with Hepatic Encephalopathy.

NCT ID: NCT02163837 Completed - Clinical trials for Hepatic Encephalopathy

Effect of Rifaximine on Sleep Disorders in Patients Suffering From Hepatic Encephalopathy

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

Hepatic encephalopathy is responsible for sleep disturbances and daytime sleepiness. The purpose of our study is to assess sleep quality, quantity, sleep schemes and physical activity in patients suffering from HE, before and after a 2 weeks treatment with rifaximine, which is currently given to lower blood ammoniac levels.

NCT ID: NCT02158182 Completed - Clinical trials for Hepatic Encephalopathy

Lactulose, L-ornithine L-aspartate, or Rifaximin Versus Placebo for Preventing Hepatic Encephalopathy in Variceal Bleeding

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

The aim of this study is to determine whether lactulose, L-ornithine L-aspartate, and rifaximin are effective in the prevention of the development of hepatic encephalopathy in cirrhotic patients with acute variceal bleeding

NCT ID: NCT02156232 Completed - Liver Cirrhosis Clinical Trials

Embolization of Large Spontaneous Portosystemic Shunts for the Prevention of Post-TIPS Hepatic Encephalopathy

Start date: June 15, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether transjugular intrahepatic portosystemic shunt (TIPS) combined with large spontaneous portosystemic shunts embolization are effective in the prevention of hepatic encephalopathy (HE).

NCT ID: NCT02154282 Completed - Cirrhosis Clinical Trials

iPod Games in Hepatic Encephalopathy

Start date: January 2013
Phase: N/A
Study type: Interventional

To see if using ipod games can improve mental functioning

NCT ID: NCT02083367 Completed - Hepatitis C Clinical Trials

Default Mode Network fMRI Maps as a Predictive Index of Hepatic Encephalopathy Outcome

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

Investigating the impact of hepatic encephalopathy on default mode networks within the brain to provide more clues with understanding the physiology of consciousness and predicting the reversibility of comatose states.

NCT ID: NCT02022137 Completed - Liver Cirrhosis Clinical Trials

Fructans, Lactitol and Lactose in Minimal Hepatic Encephalopathy

Start date: October 2013
Phase: N/A
Study type: Interventional

As an alternative for the treatment of Minimal Hepatic Encephalopathy (MHE) Agave fructans have shown prebiotic effects, and have shown to improve function of the digestive system, control and induce glycemic effect satiety. Therefore the impact of the fermentation of such prebiotic in the gut may contribute to improving health and quality of life of patients with MHE.

NCT ID: NCT02019784 Completed - Liver Cirrhosis Clinical Trials

Randomised Controlled Trial of Mechanistic Effects of Rifaximin in Cirrhosis and Chronic Hepatic Encephalopathy

RIFSYS
Start date: January 2015
Phase: Phase 4
Study type: Interventional

Patients with cirrhosis are particularly prone to infection which is frequently a precipitant of hepatic encephalopathy, renal failure and circulatory collapse. Bacterial infections are of particular concern in patients with cirrhosis because they are poorly tolerated. Sepsis and associated endotoxaemia whereby bacteria produce inflammatory particles occur in approximately 40% of hospitalized patients with cirrhosis and is a major cause of death. Gut-derived and blood-borne pathogens can induce an inflammatory response within the liver and spleen, which are the major organs that remove bacteria and their endotoxin (such as lipopolysaccharide - LPS and bacterial DNA itself) from the bloodstream. Several mechanisms have been identified and proposed in this process which depends upon a balance between the barrier functions of the gut and the 'detoxifying' capacity of the liver. People with established liver cirrhosis have been shown to have escape of endotoxin into the bloodstream produced by bacteria that reside in their intestines, which becomes more permeable or 'leaky'. Gut dysfunction is defined by changes in the types of bacteria within the gut and in overall permeability allowing bacterial products which would otherwise be contained within the gut to travel into the bloodstream and lymphatic system with detrimental effects elsewhere in the body. This passage of bacterial products is termed bacterial translocation, and it's effects on the liver and general immune system can be then be measured. It has now become recognised that certain types of white blood cells such as neutrophils and monocytes become dysfunctional and this predisposes to infection and may also have a more direct pathogenic role in hepatic encephalopathy. Thus neutrophil and monocytes may be a novel pharmacotherapeutic target in a condition where current therapies such as bowel aperients (e.g. lactulose) are inadequate. A therapeutic strategy utilising Rifaximin, a non-absorbable antibiotic, to modulate gut bacterial which produce ammonia, a chemical known to be important in the cause of hepatic encephalopathy, could potentially lower gut-derived systemic inflammation, endotoxaemia, infection and organ dysfunction in this population improving outcomes and prolonging transplant-free survival. We therefore plan to test if Rifaximin positively affects markers of immune dysfunction in patients with liver cirrhosis experiencing chronic hepatic encephalopathy after 30 days of treatment, as our primary research question. Positive results from this study would support further trials into the potential benefit of using Rifaximin to improve immune function, as well as reduce the recurrence of hepatic encephalopathy, in patients with liver cirrhosis.

NCT ID: NCT02017119 Completed - Cirrhosis Clinical Trials

Comparison Between Lactulose and Lactulose-Paraffin in Cirrhotic Patients

Start date: January 2011
Phase: Phase 2
Study type: Interventional

Hepatic encephalopathy (HE) is an important complication of liver cirrhosis. Lactulose is a first line treatment for HE, but the adherence to this treatment is relatively low, due to side effects such as diarrhea, distention, etc.