Clinical Trials Logo

Mechanical Ventilation clinical trials

View clinical trials related to Mechanical Ventilation.

Filter by:

NCT ID: NCT01233726 Completed - Critical Illness Clinical Trials

Effects of a Complete Diet in Critically Ill Patients With Stress Hyperglycemia

Start date: April 2010
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the beneficial effects of the administration of a complete diet rich in monounsaturated fatty acids and slow absorption carbohydrate in patients with stress hyperglycemia(T-Diet Plus Diabet IR). The main objective of this project is to evaluate blood glucose metabolic control, insulin requirements, insulin action resistance, lipid profile and to reduce infectious complications on mechanical ventilation ICU patients after the administration of a complete diet enriched in MUFA and slow absorption carbohydrates, without fructose.

NCT ID: NCT01204281 Completed - Respiratory Failure Clinical Trials

Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients

Start date: September 2010
Phase: Phase 4
Study type: Interventional

To evaluate the effectiveness of high assistance proportional assist ventilation (PAV+) (objective 80% gain) as main ventilatory support in early stage of critically ill patients in comparison with standard volume-assist control ventilation (ACV).

NCT ID: NCT01165606 Completed - Clinical trials for Mechanical Ventilation

Effects of Respiratory Physiotherapy in Critically Ill Patients Ventilated for More Than 48 Hours

Start date: n/a
Phase: N/A
Study type: Interventional

This study aimed to determine the impact of providing chest physiotherapy on the duration of mechanical ventilation, intensive care length of stay, intensive care and hospital mortality in mechanically ventilated patients.

NCT ID: NCT01140750 Completed - Clinical trials for Mechanical Ventilation

Variability Analysis as a Predictor of Liberation From Mechanical Ventilation

Start date: August 2007
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate if the variability of biological signals, such as heart rate and temperature, can predict weaning from mechanical ventilation in patients with failure to wean.

NCT ID: NCT00978783 Completed - Clinical trials for Mechanical Ventilation

Speech Effects of a Speaking Valve Versus External Positive End-expiratory Pressure (PEEP) in Tracheostomized Ventilator-Dependent Neuromuscular Patients

Start date: December 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Background: Many patients with respiratory failure related to neuromuscular disease receive chronic invasive ventilation through a tracheostomy. Improving quality of life, of which speech is an important component, is a major goal in these patients. The investigators compared the effects on breathing and speech of low-level positive end-expiratory pressure (PEEP, 5 cm H2O) and of a Passy-Muir speaking valve (PMV) during assist-control ventilation. Methods: Flow will be measured using a pneumotachograph. Microphone speech recordings were subjected to both quantitative measurements and qualitative assessments; these last consisted of a perceptual score and an intelligibility score determined by two speech therapists using a French adaptation of the Frenchay Dysarthria Assessment.

NCT ID: NCT00963066 Completed - Clinical trials for Mechanical Ventilation

NAV-ALI: Neurally Adjusted Ventilatory Assist in Patients Recovering Spontaneous Breathing After Acute Lung Injury

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

Evaluation of a new ventilatory mode Neurally Adjusted Ventilatory Assist "NAVA" in patients who recover spontaneous breathing after acute lung injury.

NCT ID: NCT00851617 Completed - Clinical trials for Mechanical Ventilation

Does Threshold IMT Influence Weaning?

Start date: August 2004
Phase: N/A
Study type: Interventional

Patients under threshold IMT show better conditions to weaning from mechanical ventilation than the control group.

NCT ID: NCT00824239 Completed - Clinical trials for Mechanical Ventilation

Intermittent Sedation Versus Daily Interruption of Sedation in Mechanically Ventilated Patients

Start date: September 2008
Phase: Phase 3
Study type: Interventional

Sedation is very important in critical care. Critically ill patients are submitted to many stressor factors that have potential to affect longterm outcomes. However, oversedation is associated with increased morbidity, including increased time of mechanical ventilation and ICU stay and longterm psychological complications. Daily interruption of sedation is associated with less time under mechanical ventilation and less posttraumatic stress disorder. Intermittent sedation, when compared with continuous sedation, is also associated with decreased time of mechanical ventilation. The aim of this study is to compare intermittent sedation with daily interruption. Our primary endpoint is free-days of mechanical ventilation in 28 days.

NCT ID: NCT00811629 Completed - Septic Shock Clinical Trials

Influence of Acute Respiratory Distress Syndrome (ARDS) and Severe Sepsis on sRAGE Levels in ICU Patients

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

sRAGE, the soluble form of the receptor for advanced glycation end products, is a novel marker of alveolar epithelial type I cell injury, but is also involved in acute systemic inflammation. The purpose of this observational prospective study is to determine whether sRAGE could be used in an ICU setting as a potential diagnostic and prognostic marker during ALI/ARDS, regardless of associated severe sepsis or septic shock.

NCT ID: NCT00804011 Completed - Clinical trials for Mechanical Ventilation

Automatic Tube Compensation (ATC) for Weaning Patients With Severe Neurotoxic Snake Envenoming

ATC
Start date: July 2004
Phase: N/A
Study type: Interventional

In the mechanically ventilated patient, the single greatest cause of imposed work of breathing is the resistance caused by the endotracheal tube. Commonly used maneuvers to overcome this resistance include the use of continuous positive airway pressure or pressure support.However, a new mode of ventilatory support called automatic tube compensation (ATC) delivers exactly the amount of pressure necessary to overcome the resistive load imposed by the endotracheal tube for the flow measured at the time (so called variable pressure support). The aim of this study is to evaluate whether a combination of pressure support with automatic tube compensation is superior to PS alone in weaning patients with severe neurotoxic snake envenoming.