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Brain Diseases clinical trials

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NCT ID: NCT01080144 Completed - Cirrhosis Clinical Trials

Feasibility of Critical Flicker Frequency Procedure for the Diagnosis of Minimal Encephalopathy

Start date: October 2009
Phase: N/A
Study type: Interventional

All patients eligible for TIPS (Transjugular intrahepatic portosystemic shunt) procedure will be considered for inclusion. After written inform consent, psychometric tests in order to calculate the psychometric hepatic encephalopathy (PHES) score, the gold standard for the diagnosis of minimal encephalopathy and critical flicker frequency (CFF) will be performed before the TIPS procedure. After TIPS, patients will be followed during one year and the psychometric test and CFF will be performed every 3 months. 30 patients will be included. The main endpoint is the success rate of CFF. The secondary end points are - Correlation between CFF and PHES score - Performance of CFF and PHES score to predict the occurrence of overt encephalopathy after TIPS procedure - A sample collection during TIPS procedure is also performed for validation of biomarkers

NCT ID: NCT01069133 Completed - Clinical trials for Minimal Hepatic Encephalopathy

Study of Rifaximin in Minimal Hepatic Encephalopathy

Start date: February 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Rifaximin therapy will improve brain functioning on MRI scanning and change the microbiome and metabolome.

NCT ID: NCT01059461 Completed - Clinical trials for Hypoxic-Ischemic Encephalopathy

Study of Cerebrolysin for Treatment of Infants With History of Neonatal Hypoxic Ischemic Encephalopathy

CerebroHIE
Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether nerve growth factor (cerebrolysin®) therapy will improve the psychomotor outcome in infants with moderate and severe hypoxic ischemic encephalopathy after hospital discharge.

NCT ID: NCT01059396 Completed - Clinical trials for Hepatic Encephalopathy

Study on B-blockers to Prevent Decompensation of Cirrhosis With HTPortal

PREDESCI
Start date: January 28, 2010
Phase: Phase 4
Study type: Interventional

This is a multicenter, randomized, double-blind, placebo-controlled study on the effectiveness of treatment with beta-blockers to prevent decompensation of cirrhosis with portal hypertension.

NCT ID: NCT01041755 Completed - Clinical trials for Hepatic Encephalopathy

Efficacy of L-Ornithine L-Aspartate in Acute Hepatic Encephalopathy.

Start date: November 2009
Phase: Phase 4
Study type: Interventional

Hepatic encephalopathy is caused by the effects on the brain of substances that under normal circumstances are efficiently metabolized in the liver. The hyperammonemia is the main factor responsible for the development of hepatic encephalopathy. In patients with cirrhosis, the reduction in hepatocellular function and generation of portosystemic shunts contribute to increase serum ammonium. The current therapeutic approaches, are aimed at reducing blood ammonium levels. Administration of the non-absorbable disaccharides, have become standard treatment of hepatic encephalopathy.There are no adequate clinical trials comparing the efficacy of L-Ornithine-L-Aspartate (LOLA) infusion against lactose enemas in the treatment of acute hepatic encephalopathy.

NCT ID: NCT01027715 Completed - Seizures Clinical Trials

The Impact of Electroencephalographic (EEG) Seizure Treatment in Neonatal Encephalopathy

Start date: January 2010
Phase: N/A
Study type: Interventional

This is a prospective, randomized, single-center pilot trial of term and near term (≥ 36 weeks gestation) infants with encephalopathy or seizures comparing a "EEG Seizure Treatment Group" or ESG with a "Clinical Seizure Treatment Group" or CSG. The investigators hypothesize that the accurate detection and treatment of EEG seizures will decrease the seizure burden and improve outcomes in newborn infants with seizures and/or hypoxic-ischemic encephalopathy (HIE).

NCT ID: NCT01008293 Completed - Clinical trials for Hepatic Encephalopathy

Effect of Probiotics in Treatment of Minimal Hepatic Encephalopathy (MHE) and Health Related Quality of Life

MHE
Start date: October 2009
Phase: Phase 2/Phase 3
Study type: Interventional

This study is a randomized, open, parallel group, active comparator, single center trial. Objectives of the study are hereby given below: - To study the health related quality of life (HRQOL) in patients with chronic liver disease. - To assess the prevalence of minimal hepatic encephalopathy (MHE) in patients with chronic liver disease and assessment of HRQOL in patients with MHE. - To compare the effect of probiotics and lactulose in the treatment of MHE - To assess the effect of probiotics and lactulose on the HRQOL in patients with MHE.

NCT ID: NCT00999167 Completed - Cirrhosis Clinical Trials

A Study of Safety and Efficacy of HPN-100 in Subjects With Cirrhosis and Episodic Hepatic Encephalopathy

HALT-HE
Start date: December 2009
Phase: Phase 2
Study type: Interventional

This is a phase 2 study of HPN-100 in subjects with hepatic encephalopathy (HE) consisting of an open label safety lead-in (Part A), followed by randomized, double-blind, placebo-controlled treatment (Part B).

NCT ID: NCT00992290 Completed - Clinical trials for Minimal Hepatic Encephalopathy

Probiotic Lactobacillus GG (LGG) in Patients With Minimal Hepatic Encephalopathy

Start date: October 2009
Phase: Phase 1
Study type: Interventional

This research proposes to find whether the probiotic lactobacillus GG is safe and well tolerated in patients with minimal hepatic encephalopathy. We also want to get insight into the mechanisms of action of LGG.

NCT ID: NCT00986895 Completed - Clinical trials for Hepatic Encephalopathy

A Study of Glyceryl Tri-(4-phenylbutyrate) Administered Orally as a Single Dose, and Twice Daily for Seven Consecutive Days to Subjects With Hepatic Impairment With Cirrhosis and to a Control Group

Start date: September 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of GT4P administered orally as a single dose, and twice daily for 7 consecutive days, to subjects with hepatic impairment with cirrhosis (Child-Pugh scores of A, B, or C) and to a gender matched and similar age control group with normal hepatic function.