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Hepatic Encephalopathy clinical trials

View clinical trials related to Hepatic Encephalopathy.

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NCT ID: NCT04082780 Completed - Cirrhosis, Liver Clinical Trials

Rifamycin in Minimal Hepatic Encephalopathy

RIVET
Start date: September 1, 2019
Phase: Phase 2
Study type: Interventional

This is a randomized double-blind placebo-controlled trial of MHE in patients with cirrhosis using rifamycin SV-MMX 600mg BID vs placebo for 30 days with PK, safety, microbiota, brain function and brain MRI endpoints.

NCT ID: NCT04077125 Completed - Clinical trials for Minimal Hepatic Encephalopathy

Transcranial Doppler Ultrasound and Minimal Hepatic Encephalopathy

Start date: January 18, 2018
Phase:
Study type: Observational

Minimal hepatic encephalopathy (MHE) is a subclinical complication of liver cirrhosis with a relevant social impact. Thus, there is urgent need to implement easy to use diagnostic tools for the early identification of affected patients. This study was aimed to investigate cerebral blood flow, systemic hemodynamics as well as endothelial function of cirrhotic patients with MHE, and to verify their change after treatment with rifaximin.

NCT ID: NCT04058327 Completed - Clinical trials for Hepatic Encephalopathy

A Study of MHE in Patients With Liver Diseases

Start date: May 1, 2019
Phase:
Study type: Observational

The study analyzes the diagnostic efficacy of neurophysiological tests and blood biomarkers on MHE, predicts risk factors on the development of OHE and investigate the mortality of MHE in patients with cirrhosis and acute on chronic liver failure.

NCT ID: NCT03796598 Completed - Cirrhosis Clinical Trials

FMT in Cirrhosis and Hepatic Encephalopathy

Start date: July 29, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Patients with end stage of liver disease or cirrhosis can develop confusion due to high ammonia and inflammation. This confusion is brought upon by changes in the bacteria in the bowels and may not respond to current standard of care treatments. Repeated episodes of confusion can make it difficult for patients to function and may result in multiple admissions to the hospital and burden on the family. The investigators have studied using a healthy person's stool to replace the bowel bacteria, called fecal microbial transplant, in small studies with good results. In this trial the investigators propose to perform these procedures using an upper and lower route in Veterans who suffer from this condition and follow them for safety and HE and related hospitalizations over 6 months. The investigators will compare this to placebo treatments and hope that this intervention can improve the health and daily functioning of affected patients.

NCT ID: NCT03712280 Completed - Hepatic Cirrhosis Clinical Trials

MNK6106 for Liver Disease (Hepatic Cirrhosis) That in the Past Has Affected the Brain (Hepatic Encephalopathy)

Start date: December 1, 2018
Phase: Phase 2
Study type: Interventional

The main reason for this study is to see how the study drug interacts with the body. It will compare different doses of the study drug with a drug already in use. Participants will be adults with liver disease that has affected the brain in the past.

NCT ID: NCT03663114 Completed - Clinical trials for Carcinoma, Hepatocellular

A Post-marketing Observational Study on Risk Factors for Hepatic Encephalopathy in Participants With Unresectable Hepatocellular Carcinoma

Start date: July 2, 2018
Phase:
Study type: Observational

This study is a post-marketing observational study of lenvatinib in participants with unresectable hepatocellular carcinoma. The primary objective of this study is assessment of risk factors for hepatic encephalopathy.

NCT ID: NCT03586115 Completed - Clinical trials for Hepatic Encephalopathy

Minimal Hepatic Encephalopathy in Hereditary Hemorrhagic Telangiectasian

mHE-HHT
Start date: January 8, 2018
Phase:
Study type: Observational

HHT or Rendu-Osler-Weber disease is a genetic disease with an autosomal dominant inheritance pattern, characterized by widespread telangiectases that can involve several organs including the intestinal tract and the liver. Liver involvement by HHT is characterized by widespread diffuse liver vascular malformations that give origin to arteriovenous, arterioportal and portovenous shunts. The prevalence of hepatic involvement in HHT can reach 78%. Less commonly, patients may also develop porto-systemic encephalopathy (PSE). However, there are no studies on the possibility that patients with HHT might develop mHE, a highly plausible hypothesis considering the presence of diffuse macroscopic and microscopic porto-systemic shunt in this pathological condition.

NCT ID: NCT03585257 Completed - Cirrhosis Clinical Trials

HEAL STUDY (Hepatic Encephalopathy and Albumin Study)

HEAL
Start date: June 20, 2018
Phase: Phase 2
Study type: Interventional

Patients with continued cognitive impairment after episodes of HE have few options beyond lactulose and rifaximin in the US. Therefore using IV albumin in a randomized, double-blind, placebo-controlled trial, which could beneficially impact inflammation, could be an additional approach to improve cognition. This 6 week trial will study changes in cognition, HRQOL and inflammation in patients with covert HE after prior overt HE using multiple IV albumin infusions vs. placebo.

NCT ID: NCT03515044 Completed - Clinical trials for Overt Hepatic Encephalopathy

Rifaximin Soluble Solid Dispersion (SSD) Tablets Plus Lactulose for the Treatment of Overt Hepatic Encephalopathy (OHE)

OHE
Start date: September 13, 2018
Phase: Phase 2
Study type: Interventional

Study to Assess the Efficacy and Safety of Rifaximin Soluble Solid Dispersion (SSD) Tablets Plus Lactulose for the Treatment of Overt Hepatic Encephalopathy (OHE).

NCT ID: NCT03493204 Completed - Cirrhosis Clinical Trials

Tackling 30-day Readmissions in Patients With Cirrhosis: The SALTYFOOD Trial

Start date: April 24, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility of a home meal delivery program for patients with cirrhosis and ascites and to determine the effectiveness of a salt-restricted (2 gram sodium) meal delivery program in reducing the need for therapeutic paracenteses and/or all-cause re-admissions for these patients. Many patients with cirrhosis don't have enough nutrients in the body and are frail and these meals may help them maintain a good diet and lead to improved quality of life.