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Brain Injury clinical trials

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NCT ID: NCT01059890 Completed - Brain Injury Clinical Trials

Cerebral Antibiotics Distribution After Acute Brain Injury

Start date: September 2009
Phase: Phase 1
Study type: Interventional

The aim of the study is to explore the distribution of antibiotics in the brain after an acute brain injury because brain infections treatment is still an health care problem.

NCT ID: NCT01035606 Completed - Brain Injury Clinical Trials

Training in Goal-directed Attention Regulation for Individuals With Brain Injury

Start date: September 2009
Phase: N/A
Study type: Interventional

Brain injuries affect the lives of numerous Veterans. This study examines how the brain is affected by injury and how rehabilitation training for attention dysfunction may change brain functioning.

NCT ID: NCT01021137 Completed - Brain Injury Clinical Trials

Vestibular Consequences of Blast-related Mild Traumatic Brain Injury (TBI)

Start date: May 1, 2011
Phase:
Study type: Observational

The purpose of this project is to determine the effects of mild traumatic brain injury and blast exposure on the inner ear balance and central nervous systems.

NCT ID: NCT00875329 Completed - Brain Injury Clinical Trials

Traumatic Brain Injury (TBI) Screening Instruments

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

Goal: The ultimate goal of this research program is to improve the health and quality of life for wounded warriors from Operations Enduring Freedom and Iraqi Freedom (OEF/OIF) through screening, risk assessment, and outcome measurement. Purpose: The purpose of this study is to evaluate the reliability and validity of the existing Traumatic Brain Injury (TBI) Clinical Reminder Screen for OEF/OIF Veterans.

NCT ID: NCT00830453 Completed - Stroke Clinical Trials

Hyperbaric Oxygen Therapy in Chronic Stable Brain Injury

HYBOBI
Start date: November 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to discover the feasibility of conducting clinical research in individuals with chronic sequelae following brain injury who are given hyperbaric oxygen. This study will also look at the outcome of individuals with a chronic stable brain injury due to trauma, anoxia (lack of oxygen to the brain), or stroke, who are given hyperbaric oxygen. Outcome measures testing cognitive (memory, etc.) and functional (balance, strength, etc.) measures will be performed before the hyperbaric sessions, immediately following them, and 6 months later. The subject will receive 60 hyperbaric sessions, 60 minutes in the chamber, to a pressure of 1.5 ATA, once daily, Monday through Friday.

NCT ID: NCT00817791 Completed - Brain Injury Clinical Trials

Preconditioning With Hyperbaric Oxygen in Cardiovascular Surgery

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

Animal studies have shown that preconditioning with hyperbaric oxygen can induce central nervous system and heart ischemic tolerance. This study was designed to determine the protective effect of hyperbaric oxygen preconditioning on brain and myocardium ischemia-reperfusion injury during coronary artery bypass graft surgery.

NCT ID: NCT00809055 Completed - Brain Injury Clinical Trials

MRI and Neurodevelopment in Preterm Infants Following Administration of High-Dose Caffeine

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

Over the last 30 years the survival rates for babies born prematurely have improved greatly with research. As these babies grow up, we have found that many of the premature babies have learning and movement problems. The purpose of this research is to learn why premature infants are at risk for learning disabilities and movement problems later in childhood and whether this is changed by caffeine therapy. Caffeine is often used in premature babies to help them to breathe on their own. Nearly all babies born before 30 weeks gestation receive caffeine while they are in the neonatal intensive care unit (NICU). Scientists have shown that caffeine therapy given to premature babies reduces their disabilities. We will use brain monitoring, including electro-encephalogram (EEG) and magnetic resonance imaging (MRI) to understand how the brain of a premature baby develops and whether caffeine in high doses enhances protection of the developing brain. Just as we monitor the heart and lungs to improve our care of premature babies, we wish to monitor the brain so that we can understand how to improve our care for the brain.

NCT ID: NCT00797680 Completed - Cardiac Arrest Clinical Trials

Duration of Hypothermia for Neuroprotection After Pediatric Cardiac Arrest

Start date: October 2008
Phase: Phase 2
Study type: Interventional

In this study, children who survive cardiac arrest will be evaluated whether 24 or 72 hours of whole body hypothermia (cooling) during recovery is better to help prevent brain injury and improve outcome. The investigators will also test the safety of cooling patients for 24 and 72 hours. The investigators hypothesize that 72 hours of cooling will be more beneficial than 24 hours without compromising safety.

NCT ID: NCT00779324 Completed - Brain Injury Clinical Trials

Amantadine for the Treatment of Traumatic Brain Injury Irritability and Aggression: A Multi-site Study

Start date: August 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to study the effect of amantadine on irritability and aggression caused by traumatic brain injury.

NCT ID: NCT00729261 Completed - Brain Injury Clinical Trials

A Prospective Trial of Elective Extubation in Brain Injured Patients.

Start date: August 2004
Phase: Phase 1
Study type: Interventional

Identifying the optimal time of extubation in a brain injured population should improve patient outcome. Brain injured patients usually remain intubated due to concerns of airway maintenance. Current practice argues that unconscious patients need to remain intubated to protect their airways. More recent data however suggests that delaying extubation in this population increases pneumonias and worsens patient outcomes. We designed a safety and feasibility study of randomizing brain injured patients into early or delayed extubation. The purpose was to gain insight into patient safety concerns and to obtain estimates of sample size needed for a larger study.