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Respiratory Insufficiency clinical trials

View clinical trials related to Respiratory Insufficiency.

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NCT ID: NCT00433212 Completed - Clinical trials for Respiratory Insufficiency of Prematurity

Nasal Intermittent Positive Pressure Ventilation in Premature Infants (NIPPV)

NIPPV
Start date: April 2007
Phase: Phase 3
Study type: Interventional

The machines and oxygen used to help very premature babies breathe can have side-effects, such as bronchopulmonary dysplasia (BPD). Infants with BPD get more complications (a higher death rate, a longer time in intensive care and on assisted ventilation, more hospital readmissions in the first year of life, and more learning problems) than infants who do not develop BPD. Doctors try to remove the tube in the wind-pipe that links the baby to the breathing machine as soon as possible. However, small babies get tired, and still require help to breathe. One of the standard and common techniques to help them breathe without a tube in the wind-pipe is to use simple pressure support, nasal continuous positive airway pressure or nCPAP. This supports breathing a little, but it is often not enough to prevent the need to go back on the breathing machine. Nasal intermittent positive pressure ventilation (NIPPV) is similar to nCPAP, but also gives some breaths, or extra support, to babies through a small tube in the nose. NIPPV is safe and effective, and already in use as an alternate "standard" therapy. The main research question: After being weaned from the breathing machine, is NIPPV better than nCPAP in preventing BPD in premature babies weighing 999 grams or less at birth?

NCT ID: NCT00429156 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Non-invasive Ventilation Versus Sham Ventilation in Chronic Obstructive Pulmonary Disease (COPD)

Start date: January 2007
Phase: Phase 3
Study type: Interventional

The investigators hypothesize that continuation of non-invasive ventilation (NIV) at home after an episode of acute hypercapnic respiratory failure (AHRF) treated by NIV in COPD patients would reduce the likelihood of death and recurrent AHRF requiring NIV or intubation. The investigators designed this study in a way that recruited COPD patients would be started on home NIV or sham treatment after an episode of AHRF requiring acute NIV. The patients are acclimatised to NIV application after a few days of acute use. The investigators chose occurrence of life-threatening event (recurrent AHRF and death) as the primary endpoint.

NCT ID: NCT00419458 Completed - Respiratory Failure Clinical Trials

Inspiratory Muscle Training in Ventilator Dependent Patients

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

The purpose of this study is to determine if inspiratory muscle strength training will increase the proportion of ventilator dependent patients weaned versus Sham treated patients.

NCT ID: NCT00417326 Completed - Clinical trials for Community-acquired Pneumonia

Controlled Study of ONO-5046Na in Patients With Acute Respiratory Failure Associated With Community-Acquired Pneumonia

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of ONO-5046Na in patients with acute respiratory failure associated with community-acquired pneumonia

NCT ID: NCT00412308 Completed - Spinal Cord Injury Clinical Trials

A Comparison of High vs. Low Tidal Volumes in Ventilator Weaning for Individuals With Cervical Spinal Cord Injuries

Start date: December 2006
Phase: N/A
Study type: Interventional

The study will compare outcomes between individuals with sub-acute, ventilator-dependent tetraplegia using high (20 cc/kg) vs. low (10 cc/kg) tidal volumes during mechanical ventilator support.

NCT ID: NCT00405314 Completed - Hypoxia Clinical Trials

Prehospital CPAP vs. Usual Care for Acute Respiratory Failure

Start date: July 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of continuous positive airway pressure ventilation when applied by paramedics to individuals with severe breathing difficulties in the prehospital setting.

NCT ID: NCT00405002 Completed - Respiratory Failure Clinical Trials

A Validation Study of a New System for Measuring the End Expiratory Lung Volume During Mechanical Ventilation

Start date: November 2006
Phase: N/A
Study type: Observational

In this study the investigators aim to evaluate a new system dedicated to estimate the end expiratory lung volume, by measuring the VO2-VCO2, during mechanical ventilation compared to the helium dilution technique and the computed tomography (CT) scan.

NCT ID: NCT00404430 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Protocol Chronic Obstructive Pulmonary Disease

Start date: January 11, 2007
Phase:
Study type: Observational

The main objective of the study is to evaluate the predictive factors of the endothelial function to the waning of an acute exacerbation in COPD. It will act to do a multivariate analysis to determine the respective weight of the parameters of the systemic inflammation, of the oxidative stress of the functional respiratory parameters and then functional respiratory parameters. In exacerbated Chronic Obstructive Pulmonary Disease (COPD) patients, there is augmentation of hypoxia and the obstructive ventilatory disorders is more important. This is correlated with an increase in C-reactive Protein (CRP) and of inflammatory cytokines and oxidative stress. It has been demonstrated that there is an endothelial dysfunction in answer to hypoxia. Since the exacerbated COPD patients are hypoxic in most cases , we suppose they have an endothelial dysfunction during exacerbation. So we think we will find an augmentation of vascular resistances ,shown by a peripheral arterial tone too high. And this, certainly, play a part in physiopathology of the COPD exacerbation.

NCT ID: NCT00400881 Completed - Respiratory Failure Clinical Trials

Comparison Between Two Methods of Spontaneous Breathing Trial (SBT)

Start date: January 2007
Phase: Phase 4
Study type: Interventional

To compare a new mode of mechanical ventilation, Automatic Tube Compensation (ATC) with a traditional one, Continuous Positive Airway Pressure(CPAP), on its effectiveness for detecting patients no longer needing mechanical ventilation.

NCT ID: NCT00355732 Completed - Respiratory Failure Clinical Trials

Chronic Obstructive Pulmonary Disease and Weaning From Mechanical Ventilation in Difficult to Wean Patients

Start date: n/a
Phase: Phase 4
Study type: Interventional

To evaluate and compare two methods of weaning from mechanical ventilation in patients with chronic obstructive pulmonary disease (COPD) where the extubation failed.