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Lung Injury clinical trials

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NCT ID: NCT01939067 Withdrawn - Lung Injury Clinical Trials

Infant Pulmonary Mechanics: High Flow Nasal Cannula Versus Nasal CPAP

Start date: March 2014
Phase: Phase 1
Study type: Interventional

This study is designed to evaluate the effect of heated humidified high flow nasal cannula (HHHFNC) as compared to noninvasive nasal continuous positive airway pressure (NCPAP) on lung function as a measure of lung injury in preterm infants born at 28 to 37 weeks gestation requiring continuing respiratory support.

NCT ID: NCT01936545 Recruiting - Acute Lung Injury Clinical Trials

Anesthetic Methods and Liver Transplantation

Start date: May 2011
Phase: N/A
Study type: Interventional

Postoperative pulmonary complications are not uncommon after liver transplantation. They can not only prolong the stay in intensive care unit and in hospital but also increase the morbidity and mortality rate. The underlying mechanisms are multifactorial, however, oxidative stress following hepatic ischemia reperfusion and the ensuing pulmonary leukocyte infiltration play an important part in the pulmonary complications. Various drugs and methods such as ischemic preconditioning have been used to lessen the production of oxidative free radicals following hepatic ischemia reperfusion. The choice of different anesthetic agents could aslo change the degree of production of oxygen species and antioxidant capacity during the operation. Volatile and intravenous anesthetic agents can decrease oxidative injuries through different mechanisms, however, which is better in preventing the pulmonary leukocyte infiltration is still unknown. We attempt the compare the oxidative stress and cytokine level in liver transplant recipients under desflurane or propofol anesthesia to evaluate which kind of anesthetic agent is better in this kind of surgery.

NCT ID: NCT01922557 Completed - Acute Lung Injury Clinical Trials

Thoracic Fluid Content and Acute Lung Injury

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

To study the association of the thoracic fluid content and acute lung injury during liver transplantation.

NCT ID: NCT01921101 Terminated - Acute Lung Injury Clinical Trials

Intensive Nutrition in Acute Respiratory Distress Syndrome (ARDS): A Clinical Trial (INTACT)

INTACT
Start date: July 2009
Phase: N/A
Study type: Interventional

The investigators propose a prospective randomized clinical trail to evaluate the impact of intensive medical nutrition therapy (IMNT) in patients with acute respiratory distress syndrome (ARDS) or acute lung injury (ALI) on short and long-term outcomes. Participant's (N = 200) will be randomized to receive either standard care (SC e.g. ad lib feeding of standard food) or IMNT provided early as enteral nutrition (EN) and continued as intensive diet therapy tailored to maximize oral intake until hospital discharge. Primary outcomes evaluated include infections while hospitalized, immune parameters (CD4 and CD8 cells, serum IL-10 and leptin levels, numbers of T regulatory cells and markers for T cell anergy), days on mechanical ventilation, in the ICU and hospital , and changes in fat free mass(measured by dual energy x-ray absorptiometry), weight, muscular weakness (measured as hand grip strength), fatigue (measured as distanced traveled in 6-minute walk) and pulmonary function.

NCT ID: NCT01901354 Terminated - Acute Lung Injury Clinical Trials

Acute Lung Injury Ventilator Evaluation (ALIVE)

ALIVE
Start date: November 2013
Phase: N/A
Study type: Interventional

This study will compare two ventilator modes in mechanically ventilated patients with acute lung injury. Acute lung injury (ALI) is a condition in which the lungs are badly injured and are not able to absorb oxygen the way healthy lungs do. About 25% of patients who are ventilated get ALI. ALI causes 75,000 deaths in the US each year. Ventilators can be set to work in different ways, called modes. One mode, called ARDSNet, pumps a small amount of air into the patient's lungs and then most of the air is released prior to the next breath. Another mode, called Airway pressure release ventilation (APRV), keeps air in the lungs longer between breaths. Both of these modes are currently used at this hospital. The investigators think APRV may help patients with ALI, but we do not know for sure.

NCT ID: NCT01883869 Completed - Pneumonia Clinical Trials

Targeting Platelet-Leukocyte Aggregates in Pneumonia With Ticagrelor

XANTHIPPE
Start date: June 2013
Phase: Phase 1
Study type: Interventional

The hypothesis to be tested is that ticagrelor (Brilinta™) will reduce platelet activation and markers of inflammation in patients with pneumonia.

NCT ID: NCT01814956 Terminated - Clinical trials for Parenteral Nutrition

Different Lipid Emulsions in Acute Lung Injury Patients

Start date: March 2013
Phase: Phase 4
Study type: Interventional

Aim is to investigate the influence of an early supply of parenteral nutrition including a fish oil containing lipid emulsion on the course of acute lung injury in the intensive care unit. In comparison, a standard parenteral nutrition with a soybean oil based emulsion will be used. Data obtained in this trial may provide evidence for a beneficial effect of fish oil derived omega-3 fatty acids in parenteral nutrition regarding their influence on acute lung injury.

NCT ID: NCT01783821 Active, not recruiting - Clinical trials for Acute Respiratory Distress Syndrome (ARDS)

LIPS-B: Lung Injury Prevention Study With Budesonide and Beta

LIPS-B
Start date: July 2013
Phase: Phase 2
Study type: Interventional

THE STUDY WILL ANSWER WHETHER INHALED BUDESONIDE AND FORMOTEROL ARE ABLE TO ALLEVIATE OR PREVENT PULMONARY INJURY WHEN ADMINISTERED EARLY IN HOSPITAL COURSE TO THE PATIENTS AT RISK FOR DEVELOPING ARDS

NCT ID: NCT01769053 Terminated - Acute Lung Injury Clinical Trials

Variable Pressure Support Trial

ViPS
Start date: January 2013
Phase: N/A
Study type: Interventional

In 2008 a new ventilation strategy termed variable Pressure Support ventilation (PSV) was introduced, which is able to increase the variability of the respiratory pattern independent from the inspiratory effort. In experimental lung injury, variable PSV was found to improve gas exchange and decrease the inspiratory effort, while reducing alveolar edema and inflammatory infiltration compared to conventional(non-variable) PSV. Importantly, variable PSV reduced peak airway pressure and respiratory system elastance in a variability dependent manner.In addition, preliminary observations suggest that variable PSV can reduce the work of breathing and improve patient comfort, but it is not known whether this new ventilatory strategy is able to speed the weaning from mechanical ventilation. Since variable PSV can reduce the mean pressure support, it may lead to a faster reduction of pressure support and, therefore, a shorter weaning period than conventional PSV. The hypothesis of this study is that variable pressure support ventilation reduces the duration of mechanical ventilation to non-variable (conventional) pressure support ventilation.

NCT ID: NCT01757899 Withdrawn - Clinical trials for Acute Respiratory Distress Syndrome

Effects and Safety of Infusion of Low-Doses of Methylprednisolone in Early ALI and ARDS in Children

PEDALI
Start date: January 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the effects of prolonged low-dose methylprednisolone infusion on pulmonary function (LIS and ventilation-free days), extra pulmonary organ function (PMODS score), inflammatory markers - RCP (Reactive C Protein), IL6 (Interleukine 6), TNFα (Tumor Necrosis Factor), IL8 (Interleukine 8), IL10 (Interleukine 10) and length of Pediatric Intensive Care Unit (PICU) stay in early ALI/ARDS in children.