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Acute Respiratory Failure clinical trials

View clinical trials related to Acute Respiratory Failure.

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NCT ID: NCT00871624 Completed - Clinical trials for Acute Respiratory Failure

Efficacy and Safety of Dexmedetomidine During Non-Invasive Positive Pressure Ventilation

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine the efficacy and safety of dexmedetomidine during Non-invasive positive pressure ventilation (NPPV) for patients with acute respiratory failure compared to standard analgesic/sedation practices

NCT ID: NCT00797433 Completed - Clinical trials for Acute Respiratory Failure

Outcomes of Mechanically Ventilated Patients With Low Serum Testosterone

Start date: December 2008
Phase: N/A
Study type: Observational

This is a study to determine the testosterone serum levels in male patient with acute respiratory failure requiring mechanical ventilation. The objective is to determine if low levels exist in this population and if it correlates with length of mechanical ventilation. Hypothesis: Serum testosterone levels in mechanically ventilated male patients are significantly decreased from normal levels and correlate with disease severity and outcomes.

NCT ID: NCT00780078 Completed - Heart Failure Clinical Trials

Clinical Evaluation of Swallowing Disorders as a Predictor of Extubation Failure

EVAKIN
Start date: October 2008
Phase: N/A
Study type: Observational

Patients with failed extubation stay significantly longer in an intensive care unit (ICU) and have a higher mortality rate, than those intubated successfully. Reintubation is associated with life-threatening complications and a poor prognosis. Functional respiratory tests are frequently used as weaning parameters, however, they are not accurate enough to predict extubation failure. The incidence of swallowing dysfunction is underestimated, mainly among patients whose intubation lasts longer than 48 h.We previously observed that the assessment of the swallowing function and oropharyngeal motricity, conducted by the physiotherapist before extubation could be helpful for making decisions to extubate patients intubated for over 6 days. The objective of this study is to validate a scale previously devised and used for physiotherapist bedside evaluation of the swallowing function and oropharyngeal motricity, among patients intubated for over 6 days, to determine whether this scale is a good predictor of airway secretion-related extubation failure.Expected results : to validate a scale previously devised called " physiotherapist evaluation of the swallowing function and oropharyngeal motricity before extubation" by the mean of a multicentric study. In our hypothesis the clinical parameters studied could be predictive of extubation failure. Then, this evaluation could help the medical decision in the choice of the good time for extubation. The final objective is to lower the mortality related to extubation failure.

NCT ID: NCT00632320 Completed - Clinical trials for Acute Respiratory Failure

Continuous Positive Airway Pressure and Oxygen Concentration on Measurement of Rapid Shallow Breathing Index

Start date: October 2004
Phase: N/A
Study type: Observational

To compare the rapid shallow breathing index (RSBI) values, the incidence of adverse reactions, and the predictive accuracy measured under 5 different ventilator strategies in the same patient group.

NCT ID: NCT00435110 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Effects of PEEP and FIO2 in ALI and ARDS

HELP
Start date: May 2004
Phase:
Study type: Observational

Current American-European Consensus Conference (AECC) definitions for ALI and ARDS are inadequate for inclusion into clinical trials due to the lack of standardization for measuring the oxygenation defect. We questioned whether an early assessment of oxygenation on specific ventilator settings would identify patients with established ARDS (persisting over 24h).

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: NCT00252616 Completed - Clinical trials for Acute Respiratory Failure

Timing of Target Enteral Feeding in the Mechanically Ventilated Patient

Start date: September 2003
Phase: Phase 2/Phase 3
Study type: Interventional

This study tests the hypothesis that initial trophic enteral feedings will increase the time alive and free of mechanical ventilation as compared to initial goal enteral feedings in patients who are mechanically ventilated.

NCT ID: NCT00248443 Completed - Cancer Clinical Trials

Réa-MiniMax: Severe Acute Respiratory Failure in Hematology and Cancer Patients Without Bronchoalveolar Lavage

Start date: August 2005
Phase: Phase 3
Study type: Interventional

The MiniMax® study is a multicenter randomized controlled study aimed at demonstrating that a combination of non-invasive diagnostic tools are as effective as fiberoptic bronchoscopy and bronchoalveolar lavage (FO-BAL) in performing the etiological diagnosis of acute respiratory failure in cancer patients.

NCT ID: NCT00167622 Completed - Clinical trials for Acute Respiratory Failure

Early Mechanical Ventilation for Guillain Barré Syndrome

Start date: April 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether early mechanical ventilation can prevent hospital acquired pneumonia in adults with Guillain Barré Syndrome.

NCT ID: NCT00000562 Completed - Lung Diseases Clinical Trials

Extracorporeal Support for Respiratory Insufficiency (ECMO)

Start date: June 1974
Phase: Phase 3
Study type: Interventional

To evaluate indications for the use and efficacy of extracorporeal membrane oxygenators (ECMO's) for the support of patients with potentially reversible acute respiratory failure.