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Brain Injury clinical trials

View clinical trials related to Brain Injury.

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NCT ID: NCT00453921 Completed - Brain Injury Clinical Trials

Methylphenidate (Ritalin) and Memory/Attention in Traumatic Brain Injury (TBI)

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

Traumatic brain injury (TBI) is a significant public health problem, with 1.5-2.0 million Americans injured each year. Cognitive deficits, particularly in the domains of memory and attention are frequently the source of lingering disability after TBI and a source of enormous distress to the injured individuals and their family/caregivers. To date, interventions to ameliorate chronic cognitive deficits have been directed at either pharmacological interventions or cognitive rehabilitation. We propose to (1) To compare the efficacy of three interventions: memory and attention training (MAAT), methylphenidate, and memory/attention training in combination with methylphenidate and (2) use functional MRI (fMRI) to characterize changes in activation of the neural circuitry of memory and attention due to MAAT alone, methylphenidate alone, and MAAT in combination with methylphenidate. This is a two by two design with medication (methylphenidate/placebo) and cognitive therapy (Memory and Attention Training (MAAT) or an Attention control intervention) as possible interventions. Using a randomized, placebo-controlled, double-blind design, 200 individuals with persistent cognitive deficits 6-12 months after MTBI will be randomized to receive a six week trial of either (1) MAAT and placebo, (2) MAAT and methylphenidate (0.3 mg/kg BID), (3) attention control intervention and methylphenidate (0.3 mg/kg BID), or (4) attention control intervention and placebo. Symptom distress, attention and memory performance, and activation patterns of the neural circuitry of attention and memory while undergoing fMRI will be characterized at baseline, and after the four treatment conditions. This study will provide important information on three interventions for the most disabling sequelae of an enormous public health problem. Further, it will help to clarify underlying neural mechanisms and suggest additional treatment possibilities.

NCT ID: NCT00338871 Completed - Cerebral Palsy Clinical Trials

Home Based Exercise Program for Brain Injury Children

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether simple home-base aerobic exercise program have beneficial effect on walking abilities and balance performance in children with brain damage

NCT ID: NCT00338858 Completed - Cerebral Palsy Clinical Trials

The Connection Between Gait Variability Parameters and Balance Performance in Children With Physical Disability

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the connection between gait variability parameters and balance performance in children with physical disability

NCT ID: NCT00336466 Completed - Cardiac Surgery Clinical Trials

The Erythropoietin NeuroProtective Effect: Assessment in CABG Surgery (TENPEAKS)

Start date: September 2004
Phase: Phase 2
Study type: Interventional

Context: Neurocognitive dysfunction complicates coronary artery bypass graft surgery. Neurocognitive dysfunction is a measurable problem with thinking. Erythropoietin may be a neuroprotectant. Objective: To investigate the feasibility and safety of three doses of human recombinant erythropoietin to reduce neurocognitive dysfunction in coronary artery bypass graft patients.

NCT ID: NCT00315263 Completed - Respiratory Failure Clinical Trials

Genomics, Single Nucleotide Polymorphisms (SNPs), and Clinical Neonatology

Start date: April 2006
Phase: N/A
Study type: Observational

This research seeks to establish a neonatal DNA Tissue Bank to find out if differences in small segments of DNA predispose babies to Chronic Lung Disease (CLD), Periventricular Brain Injury (PVI), Necrotizing Enterocolitis (NEC), or Hypoxic Respiratory Failure (HRF).

NCT ID: NCT00170378 Completed - Venous Thrombosis Clinical Trials

The Use of Low Molecular Weight Heparin in Traumatic Brain Injury

Start date: December 2002
Phase: Phase 4
Study type: Interventional

To study the safety and efficacy of early administration of Low Molecular Weight Heparin to patients with traumatic brain injury.

NCT ID: NCT00018499 Completed - Brain Injury Clinical Trials

Genotype Influence on Recovery After Traumatic Brain Injury

Start date: October 1998
Phase: N/A
Study type: Observational

Genetic differences in response to brain injury may reasonably be expected to play a role in the initial consequences of traumatic brain injury and in the rate of recovery from such injury.

NCT ID: NCT00006271 Active, not recruiting - Brain Injury Clinical Trials

Phase I/II Study of Neuroendocrine Dysfunction in Patients With Closed Head Injuries

Start date: January 1997
Phase: N/A
Study type: Observational

OBJECTIVES: I. Determine the incidence of neuroendocrine dysfunction in patients with closed head injuries admitted to the Transitional Learning Community in Galveston, Texas, for rehabilitation.

NCT ID: NCT00006270 Active, not recruiting - Brain Injury Clinical Trials

Study of the Approximate Entropy of Adrenocorticotropic Hormone and Cortisol Secretion in Patients With Head Injury

Start date: February 1998
Phase: N/A
Study type: Observational

OBJECTIVES: I. Determine the randomness of adrenocorticotropic hormone (ACTH) and cortisol secretion using approximate entropy in patients who have sustained a head injury. II. Determine the correlation between randomness of ACTH and cortisol secretion and stages of sleep in these patients.

NCT ID: NCT00001323 Completed - Healthy Clinical Trials

Neuropsychiatric Evaluation of Healthy Volunteers and Adults With Schizophrenia

Start date: August 1992
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the cognitive processes of participants with schizophrenia, participants with nervous system and mental disorders, and healthy volunteers. Participants in this study will undergo cognitive tests of attention, memory, attention. Participants with attention deficit hyperactivity disorder (ADHD), traumatic brain injury (TBI), bipolar disorder, and Alzheimer's disease (AD) will be compared with participants with schizophrenia. A group of healthy adults and children will undergo cognitive tests to further delineate the degree of impairment in schizophrenia and neurological disorder participants.