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Brain Injuries clinical trials

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NCT ID: NCT02465242 Recruiting - Clinical trials for Traumatic Brain Injury

Pupillometry for the Prediction of Neurologic Outcomes in Severe Traumatic Brain Injury

Start date: September 2014
Phase: N/A
Study type: Observational

Traumatic brain injury (TBI) is a major cause of morbidity and mortality in the US. The CDC states that 1.7 million people sustain a traumatic brain injury each year, with death occurring in 52,000 of these injured patients. It is also estimated that 275,000 yearly require hospitalization. The costs of TBI can be devastating to our society, with the 2010 economic cost estimated to be approximately $76.5 billion. 90% of this cost involves fatal or hospitalized brain injured patients. Furthermore, survivors of traumatic brain injury have high rates of institutionalization, readmission, and disability. The prediction of prognosis in severe TBI is a difficult problem for physicians. Prognosis evaluation in the acute phase of care varies widely among physicians caring for these patients[3]. With prognosis often in doubt, physicians have difficulty leading families and patients toward the most appropriate treatment which often leads to expensive testing and patient management. The Brain Trauma Foundation has recommended several early indicators of prognosis in severe TBI, including age, hypotension, CT scan features, Glasgow Outcome Scale score, and pupillary diameter with light reflexes. Pupillary diameter and light reflexes have been extensively studied, however accurate measurements of these prognostic factors have not been performed due to a lack of standardized measuring procedure. A new device has been validated to measure both pupil size and reactivity using infrared pupillometry. This device has also been studied to create the Neurological Pupil Index (NPi) as a measure of pupillary reactivity. The NPi has been shown to correlate with intracranial pressure readings, however there are no studies correlating the pupillometer findings with outcome measures in TBI. This study will prospectively evaluate the pupillometer readings of pupillary size and reactivity (NPi) to test the hypothesis that the NPi is a realiable predictor of 30-day outcomes in patients with severe TBI.

NCT ID: NCT02426255 Recruiting - Clinical trials for Severe Trauma (With or Without Traumatic Brain Injury)

Post Traumatic Critical Complications: a Prospective Cohort Study (ATLANREA)

Start date: March 29, 2013
Phase:
Study type: Observational

The purpose of this observational epidemiological study is to investigate the management and the complications associated with severe trauma. Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.

NCT ID: NCT02410941 Recruiting - Pulmonary Embolism Clinical Trials

Improving the Stewardship of Diagnostic Imaging Resources in Alberta Emergency Departments

Start date: January 2016
Phase: N/A
Study type: Interventional

Utilization of diagnostic imaging in the Emergency Department has increased dramatically over the past two decades, driven by an increased availability of advanced imaging, legal pressures to exclude serious diagnoses in low-risk patients, patient expectations, and the tendency to associate more testing with a higher quality of care. However, this rise in the use of diagnostic imaging, particularly in low-risk patients, may not be taking into account the risk of radiation exposure to patients, or the impact on finite health system resources. The objective of this project is to improve the appropriateness of CT imaging in Alberta Emergency Departments by advancing awareness of, and adherence to, evidence-based guidelines for CT imaging of patients with mild traumatic brain injury (MTBI) and suspected pulmonary embolism (PE). These two clinical scenarios have been selected because of evidence of significant variation in imaging practices across Alberta, and the robust evidence base that exists to guide CT imaging decisions such as the Canadian CT Head Rule and the Pulmonary Embolism Rule Out Criteria.

NCT ID: NCT02407028 Recruiting - Clinical trials for Traumatic Brain Injury

Hyperbaric Oxygen Brain Injury Treatment Trial

HOBIT
Start date: June 25, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this innovative adaptive phase II trial design is to determine the optimal combination of hyperbaric oxygen treatment parameters that is most likely to demonstrate improvement in the outcome of severe TBI patients in a subsequent phase III trial.

NCT ID: NCT02404779 Recruiting - Clinical trials for Traumatic Brain Injury

Treatment of Intracranial Hypertension of Severe Tramatic Brain Injured Patients. Physiopathologic Effects of Neuromuscular Blocking Agents

THIC Cu
Start date: March 19, 2015
Phase: Phase 4
Study type: Interventional

Severely brain injured patients are at high risk of intracranial hypertension. Among medical treatments (sedatives), neuromuscular blocking agents (NMBA) are recommended by french but not english speaking societies. Effects of NMBA are unknown. The present study is designed to compare the effects of NMBA versus placebo in the treatment of intracranial hypertension, and the underlying physiopathologic effects.

NCT ID: NCT02366754 Recruiting - Clinical trials for Traumatic Brain Injury

rTMS: A Treatment to Restore Function After Severe TBI

Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to address the need for targeted treatments that induce functional and structural changes in the brain, ultimately improving neurobehavioral functioning, the investigators propose examining the therapeutic effectiveness of repetitive Transcranial Magnetic Stimulation (rTMS). The objective is to improve functional recovery for persons remaining in vegetative (VS) and minimally conscious (MCS) states 3 to 24 months after severe TBI. The approach is to determine the neurobehavioral effect of rTMS, the relationship between neurobehavioral changes and net neural effects, and to identify and define the neural mechanisms related to neurobehavioral improvements by providing 30 active or placebo rTMS sessions.

NCT ID: NCT02341092 Recruiting - Clinical trials for Traumatic Brain Injury

Analysis and Valuation of the Expertise of Use of the Close Friends of People Victims of Traumatic Brain Injury

AVEC-TC
Start date: February 2013
Phase: N/A
Study type: Observational

Post-traumatic behavioral disorders : analysis and valuation of the expertise of use of the close friends of people victims of traumatic brain injury.

NCT ID: NCT02333006 Recruiting - Clinical trials for Traumatic Brain Injury

Anosognosia Evaluation After Cranocerebral Trauma Moderate to Severe

ANOSOGNOSIA
Start date: February 2015
Phase: N/A
Study type: Interventional

This study is conducted over 18 months. The main objective of this study is to test and compare the relevance and reliability of different tools for measuring the anosognosia. Secondary objectives are : - identify the relevant test who are able to evaluate more specially the cognitive processes involved in anosognosia - explore the links between the anosognosia manifestations and the psychological manifestations

NCT ID: NCT02322970 Recruiting - Clinical trials for Intracranial Hypertension

Invasive Versus Non Invasive Measurement of Intracranial Pressure in Brain Injury Trial (IMPRESSIT)

IMPRESSIT
Start date: July 1, 2017
Phase:
Study type: Observational

Investigators aim to assess sensitivity and specificity of transcranial doppler in ruling out intracranial hypertension in all patients admitted to intensive care unit for brain injury and needing Intracranial Pressure (ICP) monitoring (according to international guidelines). Non invasive ICP measurement through the use of transcranial doppler will be carried out before and after standard invasive ICP monitoring placement.

NCT ID: NCT02321761 Recruiting - Clinical trials for Traumatic Brain Injury

Effect of Amantadine Administration on Spatial Functioning Following Traumatic Brain Injury

Start date: June 2014
Phase: Phase 4
Study type: Interventional

Amantadine hydrochloride is one of the drugs given at rehabilitation programs to people who suffered Acquired Brain Injury in order to expedite recovery and improve functioning. A previous study examined the spatially asymmetric allocation of attention in patients with traumatic brain injury (TBI). Patients demonstrated significantly worse performance with leftward than with rightward cross-hemi field shifts of attention. This is reminiscence of neglect patients. This difference was significantly reduced during and following treatment. Our objective is to investigate whether Amantadine Hydrochloride is effective in improving allocation of spatial attention and improving function in people with Traumatic Brain Injury.