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Brain Diseases clinical trials

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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.

NCT ID: NCT00697411 Recruiting - Brain Disorders Clinical Trials

Study of Selected X-Linked Disorders: Aicardi Syndrome

Start date: October 2002
Phase:
Study type: Observational

Based on our current understanding of Aicardi syndrome, the condition is hypothesized to occur due to a genetic change on the X-chromosome. The research team is investigating Aicardi syndrome to identify the specific gene location associated with the disorder. Th investigators are collecting blood and skin biopsy samples from patients and their parents. A permanent cell line is prepared and DNA from the blood and skin samples and cell lines is isolated and then used for genetic testing. The current research includes microarray analysis which which is used to look for duplications or deletions of genetic material, mutation analysis of candidate genes by sequencing, review of medical records to identify trends suggesting possible candidate genes of interest, and X chromosome inactivation studies.

NCT ID: NCT00686920 Completed - Clinical trials for Hepatic Encephalopathy

Safety and Tolerability Study of Rifaximin in Participants With a History of Hepatic Encephalopathy

Start date: March 7, 2007
Phase: Phase 3
Study type: Interventional

This study will look at the safety of a drug used in participants who have had hepatic encephalopathy (HE) in the past.

NCT ID: NCT00655304 Completed - Clinical trials for Hepatic Encephalopathy

The Effect of Prometheus (R) Liver Support Dialysis on Cerebral Metabolism in Acute Liver Failure

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

The main objective of this study is to investigate the effect of Prometheus liver support dialysis on intracranial pressure, cerebral metabolism and circulation in patients with acute liver failure.

NCT ID: NCT00649207 Completed - Neoplasm Metastasis Clinical Trials

A Phase I Study of ABT-888 in Combination With Conventional Whole Brain Radiation Therapy (WBRT) in Cancer Patients With Brain Metastases

Start date: March 2008
Phase: Phase 1
Study type: Interventional

This Phase I clinical trial is studying the side effects and best dose of ABT-888 when given together with Whole Brain Radiation Therapy (WBRT) in treating patients with brain metastases.

NCT ID: NCT00645645 Completed - Holoprosencephaly Clinical Trials

A Study of the Genetic Analysis of Brain Disorders

Start date: June 1, 2008
Phase:
Study type: Observational

A study of the complex genetics of brain development will be undertaken with an emphasis on those genes that cause the most common structural brain anomaly in humans called holoprosencephaly (HPE). This malformation of the brain can result from either environmental or genetic causes, and it is the aim of these investigations to determine the genes responsible for both normal and abnormal brain development through the study of patients with this disorder. Mutations in one such gene, Sonic Hedgehog, have been shown by us to be responsible for approximately one quarter of familial cases of HPE. Other genes either related to the hedgehog pathway or located at unrelated defined genetic loci may also contribute to HPE and are the subject of active investigation. We anticipate that many genes important for normal brain development will be identified in the search for genetic causes of HPE.

NCT ID: NCT00624871 Completed - Clinical trials for Hypoxic Ischemic Encephalopathy

Ascorbic Acid and Ibuprofen in Infants With Hypoxic Ischemic Encephalopathy

Start date: April 2004
Phase: N/A
Study type: Interventional

Oxygen radicals and inflammation are important causes for brain injury in neonates following perinatal asphyxia. Animal studies demonstrated potential benefits to the brain when using both of vitamin C and ibuprofen. The efficacy of these 2 drugs when combined in protecting the human brain has not been studied. We aimed in this study to test the hypothesis that a combination of anti-oxidants (vitamin C) and anti-inflammatory (ibuprofen) drugs can decrease the brain injury in perinatal asphyxia and improve outcomes when given to infants immediately after birth.