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Mechanical Ventilation clinical trials

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NCT ID: NCT01270295 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Soluble Forms and Ligands of RAGE in ALI/ARDS (SoLiRAGE).

SoLiRAGE
Start date: January 2011
Phase: N/A
Study type: Observational

RAGE, the receptor for advanced glycation end products, is a novel marker of alveolar epithelial type I cell injury. Soluble RAGE (sRAGE) is elevated in the plasma and in the pulmonary edema fluid from patients with ALI/ARDS, but one should acknowledge that the RAGE/NF-B axis is also involved in the pathophysiology of various other conditions. Few data are available about the levels of soluble forms and ligands of RAGE in the setting of ALI/ARDS. The purpose of this observational prospective study is to describe soluble forms (sRAGE, esRAGE) and ligands of RAGE (HMGB-1, S100A12, AGEs) levels in ICU patients with ALI/ARDS.

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: NCT01104896 Recruiting - Smoking Clinical Trials

Effect of Daily Nicotine Patch Application on Mechanical Ventilation Weaning in Smoking Patients

NICOREA
Start date: January 2010
Phase: Phase 4
Study type: Interventional

Nicotine patches are frequently used in smoking patients during their stay in the ICU in order to avoid tobacco's weaning symptoms which are likely to interfere with mechanical ventilation weaning. Until now the effectiveness of this treatment has not been proven. The aim of this study (NICOREA study) is to determine if a difference exists on the duration of mechanical ventilation once patients receive or not a nicotine substitute.

NCT ID: NCT01104857 Active, not recruiting - Sepsis Clinical Trials

Respiratory Muscle Dysfunction in Critically Ill Patients

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

Respiratory muscle dysfunction in critically ill patients is associated with elevated morbidity, including prolonged weaning from mechanical ventilation. The causes for respiratory muscle dysfunction in these patients is poorly understood and no effective treatment is available. The general hypothesis of the present study is that in critically ill mechanically ventilated subjects respiratory muscle dysfunctions results from loss of myosin induced by activation of proteolytic cascades.

NCT ID: NCT01059929 Terminated - Critical Illness Clinical Trials

Dexmedetomidine Versus Propofol in the Medical Intensive Care Unit (MICU)

Start date: September 2009
Phase: Phase 4
Study type: Interventional

This is a randomized controlled trial to compare propofol to dexmedetomidine for prolonged sedation (> 24 hours) in critically ill patients who require mechanical ventilation.

NCT ID: NCT01047670 Recruiting - Clinical trials for Mechanical Ventilation

Septic Shock em Steroids

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

Septic shock is a frequent reason for admission on pediatric intensive care units. Interventions which can change morbidity and mortality of septic shock patients are of great interest. Steroid replacement in adults with severe sepsis and septic shock have been extensively studied. It was recently demonstrated that low dose steroid (< 300mg/ day) used for more than 5 days was associated with decreased mortality and lower requirement of vasoactive support in the adult population that had a low response to the ACTH test. However, this was not confirmed in the latest results from the CORTICUS study. Use of low dose hydrocortisone, or any other steroid has not been studied in critically ill children. Mortality associated with sepsis in children has decreased in the last decade and currently it is close to 10%, making it difficult to power a study able to show reduced mortality. Taking into account the results from previous studies reporting the high incidence of adrenal failure and its association to worse outcome, we have designed a clinical trial to evaluate the effect of low dose hydrocortisone in children with septic shock: Cortisol Replacement in Children with Sepsis Study.

NCT ID: NCT01024361 Unknown status - Clinical trials for Mechanical Ventilation

Cpap at Delivery Room for Preterm Infants

CPAP-DR
Start date: January 2009
Phase: Phase 4
Study type: Interventional

The objective of the study is to determine if CPAP applied within less than 15 min of life in the DR reduces the necessity of mechanical ventilation and surfactant during the first 5 days of life.