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Respiratory Insufficiency clinical trials

View clinical trials related to Respiratory Insufficiency.

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NCT ID: NCT00318331 Terminated - Sepsis Clinical Trials

Enteral Glutamine in Critical Illness

Start date: May 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Glutamine is an amino acid which is rapidly depleted in critical illness. It is used as energy by cells that line the gut, vital for immune system function, and works as an anti-oxidant. Glutamine supplementation has been shown to improve outcomes in ICU patients. We hypothesize that critically ill patients given extra glutamine will have less of an inflammatory response and therefore better outcomes than patients not given extra glutamine. Our study randomizes patients to tube feeding with OR without extra glutamine to see if it affects patient outcomes as well as markers of inflammation.

NCT ID: NCT00296088 Terminated - Obesity Clinical Trials

Effects of Obesity on Care and Outcomes in Mechanically Ventilated Individuals in the Intensive Care Unit

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

Obesity is a significant health care issue in the United States, particularly among the critically ill. Preliminary research has shown that differences in ventilator management exist among obese and non-obese individuals. This study will examine the effect of excess weight on ventilator management and clinical outcomes in individuals in an intensive care unit (ICU).

NCT ID: NCT00292097 Terminated - Clinical trials for Traumatic Brain Injury

A Prospective, Randomized Trial of Early Versus Late Tracheostomy in Trauma Patients With Severe Brain Injury

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

The purpose of this study is to evaluate the efficacy of early conversion tracheostomy from endotracheal intubation (ET) to percutaneous, dilatational tracheostomy (PDT) in traumatic brain-injured patients requiring prolonged mechanical ventilation.

NCT ID: NCT00243828 Terminated - Clinical trials for Respiratory Insufficiency

Assessment of the Effectivity of Total-face Mask for Noninvasive Ventilation During Acute Respiratory Failure

Start date: November 2005
Phase: Phase 4
Study type: Interventional

Total-face mask may improve the efficacy of NIV compared to conventional face mask in patients with acute respiratory failure due to enhanced tolerance and the allowance of higher airway pressure without massive leaks.MAIN OBJECTIVE: To assess, in acute respiratory failure patients, whether the total-face mask reduce the intubation rate. METHODS: 300 patients admitted in the ICU for acute respiratory failure needing continuous noninvasive mechanical ventilation. The type of mask (total-face vs. conventional face mask) will be randomized. Defined failure criteria and weaning technique will be used.

NCT ID: NCT00213395 Terminated - Clinical trials for Acute Hypercapnic Respiratory Failure

Clinical Efficacy of a Cephalic Mask for Noninvasive Ventilation During Acute Hypercapnic Respiratory Failure

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

Noninvasive ventilation (NIV) is now a major therapeutic option to manage patients with acute hypercapnic respiratory failure (AHRF). Otherwise, patient-ventilator interfaces are determinant to get an optimal NIV efficacy in parallel with ventilatory comfort. Facial masks during NIV are associated with deleterious consequences like gas leaks around the mask, skin breakdown (especially on the nasal bridge), claustrophobia and mask discomfort. In order to limit these side effects, a cephalic interface has been recently designed. Cephalic mask covers the whole anterior surface of the face and excessive mask fit pressure is therefore spread over a larger surface outside the nose area. However, this mask has a high volume that may interfere with NIV efficacy and may also induce claustrophobic sensations. The aim of this study is to compare the clinical efficacy and tolerance of a cephalic mask versus a conventional oronasal mask during AHRF.

NCT ID: NCT00208078 Terminated - Cystic Fibrosis Clinical Trials

Effect of Non-Invasive Ventilation in Cystic Fibrosis Patient With Chronic Respiratory Failure.

Start date: May 2005
Phase: Phase 4
Study type: Interventional

There is no randomised controlled trials to determine the clinical effects of long term Non-Invasive Ventilation in Cystic Fibrosis patients.

NCT ID: NCT00190346 Terminated - COPD Clinical Trials

Comparison of Humidification Devices During Non Invasive Ventilation, in Acute Respiratory Failure

Start date: December 2001
Phase: N/A
Study type: Interventional

Comparison of humidification devices during non invasive ventilation, in acute respiratory failure. The hypothesis was, due to dead space, lower humidification, a reduced efficiency of the technique (NIV) when HME are used in comparison with HH.

NCT ID: NCT00127621 Terminated - Clinical trials for Respiratory Insufficiency

Early Tracheotomy Versus Prolonged Endotracheal Intubation in Intensive Care Unit (ICU) Patients

Start date: April 2002
Phase: Phase 3
Study type: Interventional

This is a phase III trial comparing early tracheotomy versus prolonged endotracheal intubation in intensive care unit patients needing prolonged ventilatory support.

NCT ID: NCT00041561 Terminated - Clinical trials for Respiratory Insufficiency

Effects of Inhaled Nitric Oxide in the Treatment of Acute Hypoxemic Respiratory Failure (AHRF) in Pediatrics

Start date: January 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the effect of nitric oxide for inhalation on the duration of mechanical ventilation in pediatric patients with AHRF.

NCT ID: NCT00016523 Terminated - Sepsis Clinical Trials

Inhaled Nitric Oxide for Preterm Infants With Severe Respiratory Failure

Preemie iNO
Start date: January 2001
Phase: Phase 3
Study type: Interventional

This multicenter trial tested whether inhaled nitric oxide would reduce death or the need for oxygen in preterm infants (less than 34 weeks gestational age) with severe lung disease.