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Respiratory Insufficiency clinical trials

View clinical trials related to Respiratory Insufficiency.

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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: NCT00835809 Completed - Clinical trials for Acute Respiratory Insufficiency

Multi Marker Approach Interest in Emergency in Acute Respiratory Insufficiency Diagnostic

BIO-IRA
Start date: October 2008
Phase: N/A
Study type: Observational

Biomarkers have an interest in clinic diagnostic ,therapeutic and prognosis in pathophysiologic situation including cardiovascular.But interest of biomarkers in diagnostic care of severe acute respiratory insufficiency remains to clear. We propose to determine the more relevant marker combination in this case.

NCT ID: NCT00817804 Completed - Respiratory Failure Clinical Trials

Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators

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

The purpose of this study is to compare a new noninvasive ventilator to existing ventilators already used for patient care.

NCT ID: NCT00817297 Completed - Respiratory Failure Clinical Trials

Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators

Start date: January 17, 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a new noninvasive ventilator to existing ventilators already used for patient care.

NCT ID: NCT00814099 Completed - Lung Diseases Clinical Trials

Sedation Management in Pediatric Patients With Acute Respiratory Failure (The RESTORE Study)

RESTORE
Start date: January 2009
Phase: Phase 3
Study type: Interventional

People with acute respiratory failure usually require the use of an artificial breathing machine, known as a mechanical ventilator. Sedative medications, which help keep people calm and reduce anxiety, are often prescribed for children who are on mechanical ventilators. However, the longer that sedative medications are used, the longer a child may need to remain on mechanical ventilation. This study will evaluate the effectiveness of a team approach to sedation management that aims to reduce the number of days that children with acute respiratory failure require mechanical ventilation.

NCT ID: NCT00810498 Completed - Respiratory Failure Clinical Trials

Trilogy Comparison Study - Adults

Start date: March 12, 2008
Phase: N/A
Study type: Interventional

The objective of this study (Part II) will be to compare the performance of the Trilogy device and a conventional ventilator (participant's current device). Both devices will be set to the participants' current mode and prescription settings.

NCT ID: NCT00810459 Completed - Respiratory Failure Clinical Trials

Trilogy Comparison Study - Pediatrics

Start date: March 10, 2008
Phase: N/A
Study type: Interventional

The objective of this study (Part II) will be to compare the performance of the Trilogy device and a conventional ventilator (participant's current device). Both devices will be set to the participants' current mode and prescription settings.

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: NCT00784004 Completed - Clinical trials for Respiratory Insufficiency

Investigation of Efficiency of Breathing With Different Breathing Patterns

Start date: November 2007
Phase: N/A
Study type: Interventional

Our aim in this study is to investigate the efficiency of the breathing with different breathing patterns. Ten volunteers and twenty patients having respiratory problems will be coached on their breathing through specific masks which will provide four different breathing patterns. These patterns will be 1) Breathing in through the nose only and out through the mouth only 2) Breathing in through the mouth only and out through the nose only 3) Breathing in and out through the nose only 4) Breathing in and out through the mouth only The data obtained from volunteers and patients will be compared within and between the groups.

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.