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Brain Injury clinical trials

View clinical trials related to Brain Injury.

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NCT ID: NCT02240329 Completed - Brain Injury Clinical Trials

Assessment of Dystussia in Traumatic Brain Injury

Start date: March 2013
Phase: Phase 0
Study type: Interventional

The purpose of this research study is to evaluate coughing in people who have had a brain injury. It is hypothesized that individuals who have sustained a brain injury will demonstrate differences in cough waveform and respiratory measures compared to individuals who have not sustained a brain injury.

NCT ID: NCT02236065 Completed - Parkinson's Disease Clinical Trials

Combination Therapy of Cord Blood and G-CSF for Patients With Brain Injury or Neurodegenerative Disorders

Start date: August 2014
Phase: N/A
Study type: Interventional

This open label trial is conducted to investigate the efficacy and safety of the combination therapy of allogeneic umbilical cord blood (UCB) and granulocyte-colony stimulating factor (G-CSF) for patients with brain injury or neurodegenerative disorders.

NCT ID: NCT02235376 Completed - Brain Injury Clinical Trials

Criteria of Extubation Failure of Brain Injured Patients. Elaboration of a Prognostic Score.

GODWEAN
Start date: June 2013
Phase: N/A
Study type: Observational

Identification of criteria associated with extubation failure of brain injured patients. Elaboration of a prognostic score of extubation failure of brain injured patients.

NCT ID: NCT02221219 Completed - Brain Injury Clinical Trials

Effects of Delayed Cord Clamp and/or Indomethacin on Preterm Infant Brain Injury

Start date: August 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Intraventricular hemorrhage (IVH) and periventricular leukomalacia (PVL) are brain lesions that commonly occur in preterm infants and are well-recognized major contributors to long-term brain injury and related disabilities later in life. Despite its prevalence, long term consequences, and enormous medical and social costs, mechanisms of IVH and optimal strategies to prevent or treat its occurrence are poorly defined, especially for extremely premature infants. Only one medical therapy, prophylactic indomethacin during the first 3 days of life, has been shown to prevent or decrease the severity of IVH in preterm infants, but its use is limited by toxic side effects and debatable effects on long-term outcomes. Several small studies and case reports suggest that delayed umbilical cord-clamping (DCC) may also decrease the incidence of IVH in premature infants, but thus far these trials have indomethacin treatment mixed within their cord clamping protocols. The investigators are conducting a randomized, blinded investigation of 4 treatment groups: 1) Control (no intervention); 2) DCC alone; 3) Prophylactic indomethacin alone; 4) Combination of DCC/indomethacin, with respect to survival, IVH or PVL incidence and severity, neurodevelopmental outcomes, and relevant mechanistic effects. With the steady rise in extreme prematurity births and clear links of IVH to long-term disabilities there is a need to improve care for these patients. This multi- disciplinary project addresses an important medical problem for an understudied patient population, where the current practice has clear limitations.

NCT ID: NCT02215148 Terminated - Brain Injury Clinical Trials

Pharmacokinetics and Clinical Response of Tolvaptan in Neurocritical Care Patients

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

To assess the pharmacokinetic profile of tolvaptan in critically ill acute brain injury patients and to secondarily evaluate the clinical response and safety of tolvaptan in acute brain injured patients

NCT ID: NCT02136433 Recruiting - Stroke Clinical Trials

Using Tablets for Upper Extremity Rehabilitation Post Acquired Brain Injury

TBL
Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to test the effectiveness of training using novel tablet applications for hand function, compared to traditional hand exercises. In addition, we aim to examine brain plasticity following treatment with the new tablet applications. We hypothesize that training with a tablet would prove to be more effective than traditional exercises. We expect to observe neuroplastic changes in the brain in patients who practiced finger movements using the tablet.

NCT ID: NCT02123355 Not yet recruiting - Brain Injury Clinical Trials

The Effect of Dexmedetomidine to Cognition of Geriatrics in Prolonged Surgery

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

The incidence of postoperative cognitive dysfunction (POCD) is high and POCD affect the life quality and the prognosis of patients. Geriatrics is the independent risk factor of POCD, and POCD is also correlated with many other factors such as type of surgery, the duration of anesthesia and the anesthesia drugs used et al. So, the prevention and treatment of POCD in geriatrics is important. Dexmedetomidine is found to have the effect of neuro-protection, but it is controversy whether Dexmedetomidine has the effect of neuro-protection in geriatrics, especially the prolonged surgery. The purpose of this study is to explore the effect of Dexmedetomidine to the cognitive function at prolonged surgery in geriatrics in geriatrics.

NCT ID: NCT02100592 Completed - Brain Injury Clinical Trials

Early Verticalization in neuroICU With ERIGO: a Safety and Feasibility Study

Start date: October 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Severe brain injuries induce alteration of state of consciousness. These functional limitations can be significantly alleviated by treatment neurorehabilitation, particularly if this is established early. It has been shown that treatment of vertical integration in patients in a vegetative state or minimally conscious state can improve the level of supervision and positive influence on rehabilitation. Therefore, there are sufficient indications that anticipate the treatment of vertical integration, since the phase of hospitalization in ICUs, may improve the functional outcome of the patient.

NCT ID: NCT02052024 Completed - Stroke Clinical Trials

Myobloc Atrophy Study

MAS
Start date: May 2014
Phase: Phase 4
Study type: Interventional

The present pilot study is designed to assess the extent to which BOTOX and MYOBLOC cause muscle atrophy in spastic patients. The primary objective is to assess whether there is statistically significant difference in muscle atrophy between the two groups over a one year period.

NCT ID: NCT02050633 Enrolling by invitation - Brain Injury Clinical Trials

PariS -TBI Study: Paris Severe Traumatic Brain Injury Study - 8 Years

TCS8
Start date: December 2014
Phase: N/A
Study type: Observational

The objective of the protocol is to pursue the long-term follow-up of a large cohort of severe traumatic brain injury patients. This outcome is to be described in terms of activity, participation, quality of life, socio-professional outcome, economical consequences and impact on caregivers, and in relation to health care provision. Secondary objectives are to measure the impact on outcome of several predictive factors; to evaluate evolution of patients since the last (four-year) evaluation.