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Tetraplegia clinical trials

View clinical trials related to Tetraplegia.

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NCT ID: NCT01393444 Completed - Spinal Cord Injury Clinical Trials

ECoG Direct Brain Interface for Individuals With Upper Limb Paralysis

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this research study is to demonstrate that individuals with upper limb paralysis due to spinal cord injury, brachial plexus injury, amyotrophic lateral sclerosis and brain stem stroke can successfully achieve direct brain control of assistive devices using an electrocorticography (ECoG)-based brain computer interface system.

NCT ID: NCT01364480 Terminated - Spinal Cord Injury Clinical Trials

Microelectrode Brain-Machine Interface for Individuals With Tetraplegia

Start date: May 1, 2011
Phase: N/A
Study type: Interventional

The purpose of this research study is to demonstrate the safety and efficacy of using two NeuroPort Arrays (electrodes) for long-term recording of brain activity.

NCT ID: NCT01350297 Completed - Tetraplegia Clinical Trials

Diaphragmatic Reinnervation of Tetraplegic Patients With Respiratory Insufficiency

TETRADIA-UNI
Start date: March 2010
Phase: Phase 4
Study type: Interventional

This study evaluates the diaphragmatic reinnervation by inferior laryngeal nerve in tetraplegic patients with ventilatory insufficiency.

NCT ID: NCT01202019 Completed - Spinal Cord Injury Clinical Trials

Effects of Exercise in People With Tetraplegia

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

This study is designed to assess the impact of exercise and supplementation on measures of fitness, function, and cardiovascular disease risk factors/modifiers in individuals with spinal cord injury (SCI). The primary purpose of this study is to improve fitness and function, reduce cardiovascular disease risks, and enhance oxidation of dietary and body fats in persons with chronic tetraplegia through acute exercise, exercise conditioning, and dietary supplementation. This study will test the hypothesis that timing of supplementation with regards to exercise bout ('intervention/placebo') affects fitness, function, lipid profiles, lipid oxidation, and inflammatory markers after acute exercise and chronic conditioning.

NCT ID: NCT01046175 Withdrawn - Spinal Cord Injury Clinical Trials

Effect of Air-stacking on Peak Cough Flow in Patients With Acute Cervical or High Thoracic Spinal Cord Injury

Start date: February 2010
Phase: Phase 2
Study type: Interventional

Respiratory complications continue to be one of the leading causes of morbidity and mortality in people with spinal cord injury, especially among cervical and higher thoracic injuries. Both inspiratory and expiratory function are often severely decreased, leading to respiratory complications, such as atelectasis, pneumonia and ventilatory failure. The prevention of these respiratory complications needs to begin immediately after injury. To achieve effective expelling of secretions before they form mucus plugs, it is essential to improve patients ability to cough. Manually assisting the cough is one way of increasing cough flow, but an effective cough also requires adequate lung volumes. The emphasis should therefore be on expansion of the lungs before coughing. One way of expanding the lungs is by air-stacking. In air-stacking insufflations are stacked in the lungs to maximally expand them. Cough can be valued by measuring Peak Cough Flow (PCF). By combining air-stacking with manually assisted cough the PCF can be increased sufficiently. The aim of this study is to compare the effect of two different air-stacking techniques on PCF, air-stacking on a respirator versus air-stacking with a manual resuscitator.

NCT ID: NCT01024088 Completed - Respiratory Failure Clinical Trials

Prospective Study on Swallowing/Breathing Interactions in Severe Guillain Barre Syndrome.

DGVSB
Start date: March 2008
Phase: N/A
Study type: Observational

To estimate, in a longitudinal and not invasive way, in patients with SGB at respiratory risk, the function of respiratory muscles and that of the upper airways muscles by investigating the force of the tongue, the gulp, and the breath during the sleep to be able to detect bulbar impairment and establish correlations enter the various parameters to estimate better the interactions between the dysfunction of the respiratory muscles and that upper airways muscles and so determine the risk acute respiratory failure.

NCT ID: NCT01005524 Completed - Tetraplegia Clinical Trials

Brain Computer Interface for Communication in ICU: a Feasibility Study

RoBIK-1
Start date: January 2010
Phase: N/A
Study type: Observational

The main objective of this study is to evaluate the usability of a system to assist verbal communication based on BCI system using the P300 wave in patients with tetraplegia who can no longer communicate because of severe engine damage (tetraplegia) and respiratory damage requiring invasive mechanical ventilation (intubation or tracheostomy) preventing verbal communication.

NCT ID: NCT00957762 Recruiting - Diabetes Mellitus Clinical Trials

Body Composition Assessment in Spinal Cord Injury

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

The purpose of this research is to evaluate different methods of measuring body composition (amount of fat, muscle, bone, and water in your body) and to determine relationships between body composition and other medical problems associated with spinal cord injury (SCI).

NCT ID: NCT00912041 Recruiting - Clinical trials for Spinal Cord Injuries

BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia

BrainGate2
Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to obtain preliminary device safety information and demonstrate proof of principle (feasibility) of the ability of people with tetraplegia to control a computer cursor and other assistive devices with their thoughts.

NCT ID: NCT00904436 Completed - Dyspnea Clinical Trials

Evaluation of Breathing Pattern and Dyspnea in Subjects With Tetraplegia

Start date: December 1999
Phase: N/A
Study type: Interventional

Breathlessness is an extremely common and uncomfortable symptom that is reported in more than two-thirds of persons with tetraplegia. This disordered pulmonary function is due to respiratory muscle paralysis or to sympathetic denervation results in a restrictive impairment and airway hyperreactivity, respectively. These restrictive and obstructive dysfunctions have been associated with the symptom of breathlessness. However, mechanisms contributing to dyspnea in persons who have tetraplegia are not well understood. It has been demonstrated that persons with tetraplegia have an increased prevalence of breathlessness and may have an altered breathing pattern. The purpose of this study is to determine the breathing pattern at rest and measure the changes in breathing after a bronchodilator treatment (a medicine commonly used to treat asthma that relaxes and opens up airways). The determination of breathing pattern is done by measuring the movements in the chest wall while breathing. This design will elucidate differences in breathing patterns between those with tetraplegia and controls, as well as demonstrate the effect of bronchodilatation on motor drive and timing. Knowledge of the intraindividual variability and mean values of the components of the breathing pattern will improve our understanding of breathlessness in these individuals.