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Hepatic Encephalopathy clinical trials

View clinical trials related to Hepatic Encephalopathy.

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NCT ID: NCT02427906 Recruiting - Cirrhosis Clinical Trials

Effect of Transjugular Intrahepatic Portosystemic Shunt on Gut Microbiota in Cirrhotic Patients

Start date: August 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to determine the effect of transjugular intrahepatic portosystemic shunt on gut microbiota and associated inflammatory factors in cirrhotic patients.

NCT ID: NCT02401490 Recruiting - Cirrhosis Clinical Trials

Albumin Infusion Effects in Mortality in Patients With Cirrhosis and Hepatic Encephalopathy

BETA
Start date: April 2015
Phase: Phase 4
Study type: Interventional

To assess whether albumin administration after an episode of hepatic encephalopathy (≥ grade II) improves survival at 90 days (mortality endpoint treated as a composite endpoint death and/ or liver transplantation).

NCT ID: NCT02334163 Recruiting - Clinical trials for Hepatic Encephalopathy

The Effects of Nitazoxanide in Hepatic Encephalopathy

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

Evaluating the efficacy and safety of nitazoxanide in comparison to standard treatment in patients with grade II-III hepatic encephalopathy (HE). Also, Evaluating the effect of administering nitazoxanide on the improvement of patient's quality of life.

NCT ID: NCT02177708 Recruiting - Clinical trials for Hepatic Encephalopathy

Quantitative Determination of Brain Water Content in Patients During and After Hepatic Encepalopathy

Start date: January 2014
Phase: N/A
Study type: Observational

There is increasing evidence that the pathophysiology of hepatic encephalopathy (HE) is tightly associated with low-grade cerebral edema. Uptake of ammonia in astrocytes leads to osmotic swelling caused by glutamine formation. Previous studies were performed in covert HE patients or used indirect methods. Methods: The investigators wish to describes quantitative measurement of localized water content using MRI water mapping in a cohort of patients with cirrhosis during an episode of overt HE type C and again after recovery. Furthermore patients with cirrhosis and no history of HE and healthy subjects will be investigated as controls.

NCT ID: NCT01597102 Recruiting - Clinical trials for Cerebrovascular Disorders

Cerebrovascular Autoregulation During and After Liver Transplantation

dARICULtx
Start date: January 8, 2012
Phase:
Study type: Observational

The cerebrovascular autoregulation (AR) is impaired in patients with hepatic encephalopathy. Patients with the indication to liver transplantation mostly have mild to severe hepatic encephalopathy. Transplantation should recover the encephalopathy. The aim of the study is to investigate the AR during liver transplantation, with the questions if the AR is impaired at the beginning of surgery and if there are changes in AR. For follow up the AR will be measured at the first days after transplantation at the ICU.

NCT ID: NCT01356121 Recruiting - Clinical trials for Hepatic Encephalopathy

Trial Comparing Sedation for Endoscopy With Propofol Versus Midazolam in Cirrhotics

Start date: November 2010
Phase: Phase 4
Study type: Interventional

To compare effects of sedation for upper gastrointestinal endoscopy with propofol and midazolam on psychometric tests and critical flicker frequency (CFF) in cirrhotics

NCT ID: NCT01178372 Recruiting - Clinical trials for Hepatic Encephalopathy

Secondary Prophylaxis of Hepatic Encephalopathy in Cirrhosis

HE
Start date: September 2008
Phase: Phase 4
Study type: Interventional

Hepatic encephalopathy (HE), a challenging complication of advanced liver disease, occurs in approximately 30-45% of patients with cirrhosis. The treatment of choice is non-absorbable disaccharides, such as lactulose and lactitol.Probiotics are effective in the treatment of minimal hepatic encephalopathy which precipitates hepatic encephalopathy. The investigators will assess the effects of lactulose and probiotics for the prevention of recurrence of HE (secondary prophylaxis) in patients after the recovery of an episode of overt hepatic encephalopathy.

NCT ID: NCT01175538 Recruiting - Clinical trials for Hepatic Encephalopathy

Primary Prophylaxis of Hepatic Encephalopathy in Patients With Cirrhosis

Start date: January 2008
Phase: Phase 4
Study type: Interventional

To assess the effects of lactulose for the prevention of first episode of altered sensorium (hepatic encephalopathy, primary prophylaxis) in patients with cirrhosis.

NCT ID: NCT01083446 Recruiting - Clinical trials for Minimal Hepatic Encephalopathy

A Nutritional Approach to Minimal Hepatic Encephalopathy

Start date: July 2008
Phase: N/A
Study type: Interventional

This trial will study a possible effect of standard Israeli breakfast (30% of caloric value and 21 gram protein) on cognitive and executive functions (working memory, visual memory, concentration and coordination), on patients with mild-moderate liver cirrhosis.

NCT ID: NCT00553423 Recruiting - Clinical trials for Encephalopathy, Hepatic

Lactulose for the Prevention of Hepatic Encephalopathy in Cirrhotic Patients With Upper Gastrointestinal Hemorrhage

Start date: November 2007
Phase: Phase 3
Study type: Interventional

To evaluate the role of lactulose in prevention of clinically overt hepatic encephalopathy (HE) in the setting of acute upper gastrointestinal bleeding in cirrhotic patients