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Respiratory Insufficiency clinical trials

View clinical trials related to Respiratory Insufficiency.

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NCT ID: NCT01692509 Completed - Clinical trials for Respiratory Failure Requiring Non Invasive Ventilation

Non Invasive Ventilation (NIV) Related Practices, Monitoring of the NIV Treatment Effect and of the Patient's Comfort

Start date: April 2012
Phase: N/A
Study type: Observational

The practices and processes related to the administration of noninvasive ventilation (NIV) in the adult intensive care unit (ICU) of the University hospital of Lausanne will be recorded by an investigator at the bedside. The effect of the NIV treatment on various respiratory parameters ( respiratory rate, expired tidal volume, minute ventilation) will also be recorded using a pneumotachograph. Finally patient's comfort during NIV treatment will be evaluated.

NCT ID: NCT01691222 Recruiting - Heart Failure Clinical Trials

Tracheostomy in ICU With a Double Lumen Endotracheal Tube

Start date: July 2012
Phase: N/A
Study type: Interventional

Percutaneous tracheostomy in Intensive care unit (ICU) is performed with the use of flexible fiberoptic bronchoscope inside the conventional single lumen endotracheal tube owned by the patients. This situation may lead to many disadvantages for ventilation and airway protection of critically ill patients during the procedures. The use of double lumen endotracheal tube dedicated to the percutaneous tracheostomies may: 1. improve the ventilation of patients during the procedure, 2. protect the posterior tracheal wall from damage related to the different step of tracheostomies, 3. protect the lungs from blood and secretions coming down from the chosen site of tracheostomy. So the aim of this study is to evaluate the oxygenation, gas exchange, ventilation and complications of percutaneous tracheostomies performed in ICU with a dedicated double lumen endotracheal tube.

NCT ID: NCT01683526 Completed - Respiratory Failure Clinical Trials

Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope

Start date: August 2012
Phase: N/A
Study type: Interventional

The safety and efficacy of a video-laryngoscope as a primary intubation tool in urgent endotracheal intubation of critically-ill patients has not been well-described in the literature. This study will answer whether using a VL will impact on the efficacy and safety of intubation compared with a traditional direct laryngoscopy.

NCT ID: NCT01680783 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Non-Invasive Ventilation Via a Helmet Device for Patients Respiratory Failure

Start date: September 2012
Phase: N/A
Study type: Interventional

The objective of our study is to evaluate the efficacy of helmet ventilation as compared with Face mask in patients with respiratory failure.

NCT ID: NCT01675388 Withdrawn - Clinical trials for Neonatal Respiratory Failure

Hypothermia During ECMO to Decrease Brain Injury

Start date: August 2012
Phase: N/A
Study type: Interventional

Newborn infants with severe respiratory failure are treated with extracorporeal membrane oxygenation (ECMO), a modified form of cardiopulmonary bypass. These infants as at risk for brain injury as a result of hypoxia and blood flow changes in the brain prior to and during ECMO. The investigators propose a clinical trial of a novel treatment (cooling during ECMO) and novel diagnostic tool (advanced MRI techniques) that will lead to improved outcomes, early diagnosis and intervention for brain injury, decreased cost and duration of clinical trials, decrease in the burden of chronic neurologic disease and disability in society, thus improving the health and quality of life of these infants as they progress through childhood into adulthood.

NCT ID: NCT01668368 Not yet recruiting - ARDS Clinical Trials

Goal Directed Mechanical Ventilation Aimed at Optimal Lung Compliance

Start date: September 2012
Phase: N/A
Study type: Interventional

Patients with acute respiratory failure exhibiting decreased respiratory system compliance with hypoxemia or carbon dioxide retention are often difficult to ventilate with current guidelines that limit applied plateau pressure Yet, these guidelines do not take into consideration chest wall mechanics. The investigators sought to determine whether partition of the respiratory system into its components by measuring esophageal pressure and thus assessment of pleural pressure, would help in patients with acute respiratory failure to identify the factors contributing to low respiratory system compliance.

NCT ID: NCT01666834 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Cross-section Survey of Mechanical Ventilation and Acute Respiratory Distress Syndrome in China

Start date: July 2012
Phase: N/A
Study type: Observational

The characteristics and outcomes of a mixed group of critically ill patients who received mechanical ventilation are not known in China. A 1 month Cross-section survey will be performed with the aim of describing the characteristics and outcomes of conventional mechanical ventilation and treatment of acute respiratory distress syndrome in intensive care units in China.

NCT ID: NCT01663480 Completed - Respiratory Failure Clinical Trials

To Identify the Proportionality of Respiratory Work Under Different NAVA Level

Start date: March 2011
Phase: N/A
Study type: Observational

The primary purpose of mechanical ventilation is to sufficiently unload the respiratory muscles and maintain adequate ventilation in spontaneously breathing patients. When the mechanical ventilatory assist is synchronized to the patient's inspiratory effort, both the patient and the mechanical ventilator will contribute to the lung-distending pressure, necessary to overcome inspiratory load and generate the tidal volume (Vt). Unfortunately, conventional modes of mechanical ventilation cannot quantify the impact of the ventilatory assist performed by the ventilator and the patient. Inadequate levels of assist are associated with adverse effects such as development of fatigue or patient-ventilator dissynchrony and diaphragm impairment, and over assist also lead to diaphragm atrophy and weaning delay. The newly introduced neurally adjusted ventilatory assist (NAVA) has made it possible to measure the neural activity of the respiratory centers (expressed by the diaphragm electrical activity, EAdi). EAdi is a validated variable to quantify the neural respiratory drive, little is known about its usefulness to evaluate the contribution of the patient's inspiratory muscle effort relative to that of the mechanical ventilator, which would be of crucial importance to appropriately titrate the level of assist. During NAVA, the patient's efficiency to transform neural effort (EAdi) into Vt, expressed as neuroventilatory efficiency (NVE), may be a useful predictor for determining the contribution of the patient and the ventilator to generate a breath.

NCT ID: NCT01659268 Completed - Respiratory Failure Clinical Trials

Performance of Baccalaureate Nursing Students in Insertion of Laryngeal Mask: a Trial in Mannequins

LMANURSING
Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare if there difference in acquisition of knowledge and skills in airway management to baccalaureate nursing students submitted to different learning strategies: exhibition-dialogued class and practical activity in skill lab with low-fidelity mannequin or simulation class with low-fidelity mannequin.

NCT ID: NCT01645358 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Helmet Ventilation in Acute Hypercapnic Respiratory Failure

Start date: July 2012
Phase: Phase 4
Study type: Interventional

Lack of tolerance to the treatment, makes the interface choice for non-invasive ventilation (NIV) one of the key factor. To date the helmet is rarely used in Acute Hypercapnic Respiratory Failure (AHRF), because of its large dead space, despite in hypoxic respiratory failure, it is largely employed as a "rotating" strategy when the facial mask is poorly tolerated. In a multicenter randomized controlled trial, the investigators will compare the clinical efficacy of a new helmet designed to specifically improve the performance in chronic obstructive pulmonary disease (COPD) versus a full face mask during an episode of AHRF.