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Brain Injuries, Traumatic clinical trials

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NCT ID: NCT00703495 Completed - Brain Injuries Clinical Trials

Invasive and Non-Invasive Assessment of Cerebral Oxygenation in Patients With Severe Traumatic Brain Injury (TBI)

Start date: July 2008
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the relationship among regional transcranial oxygen saturation (rSO2), brain tissue oxygen pressure (PbtO2) and cerebral perfusion pressure (CPP) in patients with severe traumatic brain injury (TBI).

NCT ID: NCT00693121 Completed - Clinical trials for Traumatic Brain Injury

Amantadine for Treatment of Symptoms of the Post-traumatic Confusional State

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Patients with traumatic brain injury often experience a period of acute confusion that may include agitation as they recover from their injuries. While this confusion generally resolves with time, patients may pose increased risk of injury to themselves or others during this period. Their behavior may also increase stress for family members and interfere with their ability to benefit from rehabilitation therapies. A number of different medications have been used to treat confusion to decrease agitation, decrease risk of injury, and improve participation in rehabilitation therapies. To this point, there has not been a research or scientific basis for knowing which medication is the best for a specific patient. The overall goal of this study is to conduct a scientific investigation to help determine which medication works best to treat confusion. Study hypothesis: Amantadine will reduce the severity and number of symptoms of acute confusion after traumatic brain injury.

NCT ID: NCT00653640 Completed - Clinical trials for Traumatic Brain Injury

Physical Work Capacity After Traumatic Brain Injury

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

The purpose of this study is to determine whether body weight supported treadmill training is more effective than traditional physical therapy at restoring gait in persons recovering from traumatic brain injury.

NCT ID: NCT00627250 Completed - Clinical trials for Traumatic Brain Injury

Utility of Amantadine Hydrochloride in the Treatment of Post-traumatic Irritability

Start date: March 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if amantadine hydrochloride given 100 mg in the morning and at noon is safe and effective in the treatment of mood and behavior changes (i.e. irritability) after sustaining traumatic brain injury.

NCT ID: NCT00621751 Completed - Clinical trials for Traumatic Brain Injury

Carbamazepine for the Treatment of Chronic Post-Traumatic Brain Injury Irritability and Aggression

Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if carbamazepine reduces irritability and aggression among individuals with traumatic brain injury

NCT ID: NCT00580918 Withdrawn - Clinical trials for Mild Traumatic Brain Injury

Functional MRI Study of Attention in Normal Controls and Traumatic Brain Injured Patients

Start date: October 2003
Phase:
Study type: Observational

The purpose of this study will be to assess the attentional ability of patients with mild to moderate traumatic brain injury (TBI) using the functional Magnetic Resonance Imaging (fMRI) technique. Methodology for specific aim 1: sagittal pilot scan, 3-D anatomical MRI, Whole brain echo-planar imaging (EPI), and functional MRI techniques with traumatic brain injured subjects doing a Continuous Performance Test (CPT) attention task and compare the pattern of activation with those of normal controls to see if there is a failure to activate frontal lobes in the traumatic brain injured subjects.

NCT ID: NCT00576147 Completed - Clinical trials for TBI (Traumatic Brain Injury)

A Multi-Center Study of Near-Infrared Spectroscopy (NIRS) for Hematoma Detection

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

The purposes of this study are: 1. To determine the sensitivity and specificity of the Near-Infrared Spectroscopy (NIRS) measurements for identifying intracranial hematomas due to trauma. 2. To determine the reproducibility of the Near-Infrared Spectroscopy (NIRS) measurements with different operators and at different centers

NCT ID: NCT00557076 Completed - Clinical trials for Traumatic Brain Injury

The Efficacy of Familiar Voice Stimulation During Coma Recovery

FAST
Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether familiar vocal stimulation, provided during coma recovery, improves outcomes for persons who are unconscious after severe TBI. The primary hypothesis is that unconscious persons who receive standard rehabilitation (SR) plus a high-dose of Familiar Voice stimulation (FVs) compared to unconscious persons who receive SR plus a sham stimulation (Sham Group) will demonstrate: 1. Significantly more neurobehavioral functioning post-intervention compared to pre-intervention. 2. Using Functional Magnetic Resonance Imaging (fMRI), significantly higher average measures of volumetric activity in the whole brain, middle temporal gyrus bilaterally, primary auditory area, bilateral pre-frontal cortex, hippocampus and/or the cerebellum post-intervention compared to pre-intervention.

NCT ID: NCT00554801 Completed - Clinical trials for Traumatic Brain Injury

Central Auditory Processing Disorders Associated With Blast Exposure

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

The incidence of central auditory dysfunction in war fighters who are exposed to high-explosive blasts while serving in combat have not been clearly determined. The objectives of this study are to determine whether central auditory processing (CAP) disorders are associated with exposure to high-explosive blasts. This study will also examine the incidence, magnitude and timing of spontaneous recovery of CAP function from blast exposure. The information provided by this study will help guide clinicians in both the military and VA health care systems regarding the likelihood of central auditory processing disorders in soldiers returning from deployment and suggest some clinical rehabilitative strategies for the treatment of these patients with CAP deficits.

NCT ID: NCT00522496 Recruiting - Clinical trials for Brain Injuries, Traumatic

Proteomics of Severe Traumatic Brain Injury: A Feasibility Study

Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this study is to: 1. Determine the temporal course of matrix metalloproteinase (MMP) expression in patients wiht severe traumatic brain injury 2. Determine the temporal course of the expression of MMP-related inflammatory mediators of secondary injury in patients with severe traumatic brain injury 3. Describe the association of physiological changes and standard microdialysis analyte measures (lactate, pyruvate, lactate/pyruvate ratio, and glucose) to MMP and neuroinflammatory marker concentrations.