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Brain Diseases clinical trials

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NCT ID: NCT00862459 Completed - Brain Diseases Clinical Trials

Dose Finding Study of Gadavist in Central Nervous System (CNS) Magnetic Resonance Imaging (MRI)

Start date: August 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to look at the safety (what are the side effects) and efficacy (how well does it work) of Gadavist when used for taking images of the brain and spine. The results of the MRI with Gadavist Injection will be compared to the results of MR images taken without contrast and with the results of the MR images taken with OptiMARK.

NCT ID: NCT00839358 Completed - Sepsis Clinical Trials

Effect of Midodrine and Albumine in the Prevention of Complications in Cirrhotic Patients Awaiting Liver Transplantation

MACHT
Start date: August 2008
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the effect of prolonged administration of albumin and midodrine on the prevention of complications (renal failure, sepsis, hemorrhage, hepatic encephalopathy and hyponatremia) in patients with cirrhosis in the waiting list for liver transplantation. One hundred and ninety four patients with cirrhosis and awaiting a liver transplantation will include in the study. Patients will be randomized to receive albumin and midodrine (treatment group) or administration of placebo (saline for albumine) and tablets with excipients without midodrine (control group). Patients will be followed-up during 12th months. In the treatment group albumin will be given at a dose of 40g every 15 days and midodrine 5mg tid, in addition with lactitol (conventional doses) and the specific treatment that patients require by cirrhosis. The group control will receive placebo in the same way than the treatment group in addition with lactitol and the specific treatment that they require by their disease. In all the patients liver and renal function test, hormones determination (renin, aldosterone, noradrenaline), and cytokines will be determined in basal conditions. All these determinations will be repeated at month 1st,3rd, 6th and 12th months. Before the inclusion in the study neuropsychological test and critical flicker test will be performed to diagnose minimum EH. These tests will be repeated at 3rd, 6th and 12th months. All the determinations will be repeated at any time that the patients develop any complication considered as an end point. In baseline conditions and at 3rd and 6th months a questionnaire of quality of life (SF36) will be performed. During a year of follow-up the number of paracentesis that patients require, the incidence of renal failure and EH and their relationship with hormonal activity and cytokine levels, free transplant survival and quality of life will be recorded.

NCT ID: NCT00831337 Completed - Liver Cirrhosis Clinical Trials

Evaluation of Probiotics in the Treatment of Portal Hypertension

Start date: April 2007
Phase: N/A
Study type: Interventional

This study is to evaluate the role of probiotics in the treatment of portal hypertension. In particular the role of probiotics on gut microbiota in liver cirrhosis patients will be studied and compared with cytokines and other substances implicated in the pathogenesis of portal hypertension. The hypothesis whether probiotics may change the prognosis of patients with portal hypertension will be studied. The hypothesis whether probiotics may halt the pathologic cascade of events leading to various complications (e.g. hepato-renal syndrome, spontaneous bacterial peritonitis, bleeding varices) will be reviewed.

NCT ID: NCT00829361 Completed - Stroke Clinical Trials

Stroke Telemedicine for Arizona Rural Residents Trial

STARR
Start date: October 2008
Phase: N/A
Study type: Interventional

The STARR network registry consists of a 4 spoke 1 hub system. Which will consist of prospective collection, recording, and regular analysis of telestroke patient consultation and care data for the purpose of quality measure assessment and improvement and benchmarking against other national and international telestroke programs.

NCT ID: NCT00817401 Completed - Clinical trials for Hypoxic-Ischemic Encephalopathy

Systemic Hypothermia Improves Outcome of Hypoxic-Ischemic Encephalopathy

Start date: July 2002
Phase: Phase 1/Phase 2
Study type: Interventional

Perinatal asphyxia-induced brain injury is one of the most common causes of morbidity and mortality in term and preterm neonates. Birth asphyxia accounts for 23% of neonatal deaths globally and survivors suffer from long term neurological disability and impairment. Although many neuroprotective strategies appeared promising in animal models, most of them were not feasible and effective in human newborns. However, hypothermia was reported not to be effective if introduced beyond and thus should be introduced within 6 hrs after birth.Applying this selection criterion naturally would deprive many patients of the opportunity of hypothermia treatment.

NCT ID: NCT00808704 Completed - Clinical trials for Hypoxic-Ischemic Encephalopathy

Neurological Outcome After Erythropoietin Treatment for Neonatal Encephalopathy

Start date: August 2003
Phase: Phase 1/Phase 2
Study type: Interventional

Perinatal asphyxia-induced brain injury is one of the most common causes of morbidity and mortality in term and preterm neonates, accounting for 23% of neonatal deaths globally. Although many neuroprotective strategies appeared promising in animal models, most of them have failed clinically. Erythropoietin (EPO) is an endogenous cytokine originally identified for its role in erythropoiesis. Clinical trial has demonstrated the safety and efficacy of recombinant human erythropoietin (r-hu-EPO) in the prevention or treatment of anemia of prematurity. To date, there are no reports evaluating possible effects of EPO on neonatal HIE.

NCT ID: NCT00772096 Completed - Sepsis Clinical Trials

Septic Encephalopathy and Late Cognitive Dysfunction

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

Delirium and long-term cognitive dysfunction are important problems in intensive care patients. Patients with sepsis are at a high risk of developing delirium (septic encephalopathy), which may be an important risk factor for the development of long-term cognitive dysfunction. Working hypotheses: 1. Septic encephalopathy and cognitive dysfunction are caused by an unspecific reaction of the brain to an intense inflammatory stimulus. 2. It is possible to therapeutically influence the inflammatory response and its effects on the brain.

NCT ID: NCT00764049 Completed - Cirrhosis Clinical Trials

Single Pass Albumin Dialysis in Patients With Cirrhosis

DACAR
Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to determine whether a simplified device of albumin dialysis also has beneficial effects.

NCT ID: NCT00740142 Completed - Clinical trials for Hepatic Encephalopathy

Efficacy of Combined Oral L-ornithine-L-aspartate and Lactulose in Patients With Hepatic Encephalopathy

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

Hypothesis: Is the combination of oral L-ornithine-L-aspartate and lactulose more efficacious than oral lactulose alone in treatment of hepatic encephalopathy? Study design; Randomized, double-blinded, placebo controlled trial

NCT ID: NCT00719407 Completed - Clinical trials for Hypoxic-ischemic Encephalopathy

Neonatal Erythropoietin in Asphyxiated Term Newborns

NEAT
Start date: January 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and pharmacokinetics of moderate to high doses of erythropoietin in newborn infants with birth asphyxia.