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Lung Injury clinical trials

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NCT ID: NCT01195428 Withdrawn - Acute Lung Injury Clinical Trials

Simvastatin Effect on the Incidence of Acute Lung Injury/Adult Respiratory Distress Syndrome (ALI/ARDS)

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

Acute Lung Injury/Acute respiratory distress syndrome (ALI/ARDS) is a serious and frequently encountered entity in modern ICUs. Sepsis remains the most common cause of ALI/ARDS and carries the worst prognosis. The disease is characterized by an intense inflammatory process. This inflammation plays a major role in the development of gas exchange abnormalities seen in the course of the disease. Statins, primarily used as lipid-lowering agents, are now known to possess anti-inflammatory, antioxidant, antithrombogenic and vascular function-restoring actions. Therefore the investigators propose to determine if Simvastatin may be useful in decreasing the incidence of this deadly syndrome in critically ill patients.

NCT ID: NCT01194895 Completed - Acute Lung Injury Clinical Trials

A Trial to Evaluate the Impact of Lung-protective Intervention in Patients Undergoing Esophageal Cancer Surgery

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

The purpose of this trial is to determine whether low tidal volume during intraoperative one-lung ventilation could decrease the incidence rate of postoperative acute lung injury compared to "normal" tidal volume.

NCT ID: NCT01187004 Completed - Sepsis Clinical Trials

Extracardiac Complications After Cardiac Surgery

Start date: April 2007
Phase: N/A
Study type: Observational

Hypothesis of the study is that patients undergoing major cardiac surgery can develop extracardiac complications correlated to cardiopulmonary by pass.

NCT ID: NCT01186874 Unknown status - Clinical trials for Acute Respiratory Distress Syndrome

Epidemiology Research on Acute Lung Injury/Acute Respiratory Distress Syndrome (ALI/ARDS) in Adult ICU in Shanghai

Start date: September 2010
Phase: N/A
Study type: Observational

To survey the prevalence and the mortality of the Acute Lung Injury/ Acute Respiratory Distress Syndrome (ALI/ARDS) in 12 university hospital ICUs in Shanghai.

NCT ID: NCT01184313 Not yet recruiting - Lung Injury Clinical Trials

Acute Lung Injury After Aortic Valve Surgery

Start date: September 2010
Phase: N/A
Study type: Observational

The purpose of this prospective, randomized clinical trial is to understand and measure lung injuries caused by CPB in aortic valve surgery. Study questions: - Is there any correlation between the release of pro-inflammatory biomarkers and lung injury degree? - Is there any correlation between oxyhaemodynamic parameters and lung injury degree? - Is there any correlation between oxyhaemodynamic parameters and the release of pro-inflammatory biomarkers? - Are budesonide, erdostein and acetylcystein effective in the prevention of lung injuries?

NCT ID: NCT01170845 Completed - Esophageal Cancer Clinical Trials

Effect of Neutrophil Elastase Inhibitor on Lung Injury After Esophagectomy

NEIE
Start date: March 2007
Phase: N/A
Study type: Interventional

A neutrophil elastase inhibitor may have effect on suppression of the lung injury after thoransthoracic esophagectomy. The investigators hypothesized that postoperative complication, particularly respiratory complication may be reduced by neutrophil elastase inhibitor after esophagectomy.

NCT ID: NCT01159392 Completed - Acute Lung Injury Clinical Trials

Alveolar Recruitment in Brain Injury

Start date: February 2001
Phase: N/A
Study type: Observational

Development of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) in patients with severe brain injury has been associated with poor outcome. The application of lung recruitment maneuvers (RM) for a short period of time to open collapsed alveoli and reverse hypoxemia in early ARDS has been recommended. However, little is known about the cerebral and vascular effects of RM in brain injury patients with ALI/ARDS. The aim of this study is to assess the effects of a single standardized RM on oxygenation and on systemic and cerebral hemodynamics in severe brain injury patients with ALI/ARDS.

NCT ID: NCT01150864 Completed - Acute Lung Injury Clinical Trials

Effects of Airway Conditioning Devices on Ventilator Associated Pneumonia:a Randomized Clinical Trial

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

The main hypothesis are: 1. Passive and Active-Passive airway conditioning devices reduce the incidence of ventilator associated pneumonia 2. Active-Passive airway conditioning devices reduce the incidence of endotracheal tube obstruction 3. Nurses' workload is reduced with Passive and Active-Passive airway conditioning devices

NCT ID: NCT01144585 Completed - Acute Lung Injury Clinical Trials

Effects of Remote Ischemic Preconditioning and Postconditioning on Lung Injury During Cardiopulmonary Bypass

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

Remote Ischemic Preconditioning(RIPC) and remote ischemic postconditioning(RIPoC) seems to have a protective effect during ischemic period. Using cardiopulmonary bypass(CPB) during open heart surgery reduces pulmonary blood flow and may cause ischemic damage to lung tissue. The investigators anticipate that RIPC and RIPoC may reduce lung injury after CPB.

NCT ID: NCT01142544 Completed - Children Clinical Trials

Incidence of Acute Lung Injury in Children

PED-ALIEN
Start date: February 2010
Phase: N/A
Study type: Observational

Acute lung injury in children is a syndrome of rapid onset of acute respiratory failure and require admission into intensive care units (ICU) for advanced life support. There are almost no information on epidemiology of acute lung injury. Published studies do not have information for an entire year and none of them have evaluated the degree of oxygenation failure under standard ventilator settings. The investigators will perform a 1-year prospective audit of all patients admitted with acute lung injury in a network of pediatric ICUs in Spain.