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Brain Injuries clinical trials

View clinical trials related to Brain Injuries.

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NCT ID: NCT01786460 Completed - Clinical trials for Brain Injuries, Traumatic

Brain Injury Biomarkers in the General Population

Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of this study is to use an investigational assay to assess levels of putative biomarkers of traumatic brain injury (TBI) in a general population. The data will be used in a correlative analysis with data collected under a separate study of severe TBI.

NCT ID: NCT01786447 Terminated - Clinical trials for Brain Injuries, Traumatic

Biomarkers of Brain Injury: Magnitude and Outcome of Mild and Moderate TBI

Start date: April 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine if specific brain injury biomarkers have utility as blood-based traumatic brain injury (TBI) diagnostic and monitoring tools. This will be accomplished by examining the relationships between potential serum-based TBI biomarkers and clinical measures of injury severity, occurrence of complications, and outcome, in subjects with mild or moderate TBI as well as in orthopedic control subjects.

NCT ID: NCT01779427 Withdrawn - Brain Concussion Clinical Trials

Attention Intervention Management

AIM
Start date: January 2013
Phase: N/A
Study type: Interventional

This is a research study to learn if a computer-based intervention that provides direct attention and metacognitive strategy development can improve attention, memory, and executive control in adolescents with moderate-to-severe TBI who are experiencing attention difficulties post injury.

NCT ID: NCT01768650 Completed - Chronic Pain Clinical Trials

Structured Treatment of Pain (STOP) Study

STOP
Start date: June 2014
Phase: N/A
Study type: Interventional

This study seeks to compare two different behavioral treatments for pain in Veterans with a history of TBI. Both treatments involve educating the Veteran about pain, discussing the impact of pain, and different ways to manage it in hopes of decreasing pain and its impact on life. These approaches are called "self-management" approaches to pain. Both of these treatments are commonly used in pain clinics to treat pain in persons with back pain, headaches, and other types of chronic pain. The investigators will be delivering both treatments over the telephone to make the treatments accessible to Veterans wherever they live.

NCT ID: NCT01763892 Completed - Clinical trials for Traumatic Brain Injury

Physiologic Mechanisms in Pediatric Traumatic Brain Injury (TBI)

Start date: December 2012
Phase: N/A
Study type: Observational

The aims of this study explore the relationships between cerebral vasospasm, apolipoprotein-E (apo-E) genotype, physiologic symptoms, and neurocognitive outcomes that may either intensify or ameliorate secondary injury, for children with a traumatic brain injury. Exploring the apo-E genotype will help us know if injury response is altered in certain children and will aid in developing interventional approaches.

NCT ID: NCT01762475 Completed - Clinical trials for Traumatic Brain Injury

Sildenafil for Cerebrovascular Dysfunction in Chronic Traumatic Brain Injury.

Start date: January 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether sildenafil (Viagra®) is effective in improving cerebral blood flow and cerebrovascular reactivity inpatients who have persistent symptoms at least 6 months after a traumatic brain injury (TBI).

NCT ID: NCT01760785 Completed - Alcoholism Clinical Trials

Valproate for Mood Swings and Alcohol Use Following Head Injury

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

Successful treatment of traumatic brain injury (TBI)-induced mood lability may reduce or eliminate drinking behaviors in persons with alcohol abuse/dependence (AA/D) and affective lability following TBI. Observed clinically, the symptoms of poorly regulated affective expression of AA/D+TBI patients who reach alcohol abstinence do not appear to be those of an idiopathic mood or anxiety disorder. These symptoms do not present the severity or the same natural courses as do Major Depressive Disorder, Bipolar Illness, or Anxiety Disorder, for example. Instead, both symptoms and course appear more characteristic of the sustained affect lability often observed following TBI. This observation suggests that TBI survivors represent a patient group for whom treatment of neuropsychiatric symptoms following TBI may alleviate both TBI-related affect lability and also heavy ethanol use by treating the condition that is contextually related to excessive alcohol use. Based on this concept of consequently treating AA/D through the management of post-TBI affective lability, this study was conducted observing the efficacy of divalproex sodium on the severity of affective lability and AA/D in persons suffering from a moderate TBI. Divalproex sodium has been shown to ameliorate mood disorders, even in those with substance abuse problems. This drug has also shown positive results as an alternate medication to benzodiazapines in the treatment of alcohol withdrawal, significantly reducing the progression of withdrawal symptoms in patients.

NCT ID: NCT01759173 Completed - Clinical trials for Minor Traumatic Brain Injury (TBI)

Evaluate the Effectiveness of Brain Network Activation (BNA™) Technology in the Management of Sport Related Concussion

Start date: September 2012
Phase: N/A
Study type: Observational

Currently, there is no direct, reliable, bed-side, and non-invasive method for assessing changes in brain activity associated with concussion. Event Related Potentials (ERPs), which are temporal reflections of the neural mass electrical activity of cells in specific regions of the brain that occur in response to stimuli, may offer such a method, as they provide both a noninvasive and portable measure of brain function. The ERPs provide excellent temporal information, but spatial resolution for ERPs has traditionally been limited. However, by using high-density electroencephalograph (EEG) recording spatial resolution for ERPs is improved significantly. The paradigm for the current study will combine neurophysiological knowledge with mathematical signal processing and pattern recognition methods (BNA™) to temporally and spatially map brain function, connectivity and synchronization. The proposed study will provide additional evidence for the utility and contribution of the BNA™ test (reflecting temporal and spatial changes in brain activity as well as brain functional connectivity associated with concussion) in concussion management.

NCT ID: NCT01754883 Withdrawn - Clinical trials for Mild Traumatic Brain Injury

Lithium Augmentation for Hyperarousal Symptoms of Post Traumatic Stress Disorder: Pilot Study

Start date: January 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to explore the effectiveness of adding lithium carbonate (lithium) to treatment for combat-related post traumatic stress disorder in combat veterans. The goal of this study is to establish that lithium is a practical and tolerable treatment option for veterans with combat posttraumatic stress disorder.

NCT ID: NCT01750268 Completed - Clinical trials for Traumatic Brain Injury (TBI)

Topiramate Treatment of Hazardous and Harmful Alcohol Use in Veterans With TBI

VAT
Start date: November 2012
Phase: Phase 4
Study type: Interventional

The goal of the proposed project is to improve the treatment of veterans with co-occurring traumatic brain injury (TBI) and hazardous or harmful alcohol use. The PI and coinvestigators will conduct a pilot controlled clinical trial of topiramate for the treatment of these co-occurring disorders.