Clinical Trials Logo

Lung Injury clinical trials

View clinical trials related to Lung Injury.

Filter by:

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: 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.

NCT ID: NCT01114009 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Effects of Recruitment Maneuvers in Early Acute Lung Injury (ALI) and Acute Respiratory Distress Syndrome (ARDS) Patients

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

The purpose of this study is to evaluate the effect of lung recruitment maneuver in patients with early ALI/ARDS

NCT ID: NCT01105663 Completed - Clinical trials for Pediatric Acute Lung Injury

Pharmacologic Impact on Sedation Assessments

PISA
Start date: March 2010
Phase: N/A
Study type: Observational

PISA is an ancillary study to the NIH funded clinical RESTORE Trial (U01 HL086622). This study will provide data that may allow for improved dosing recommendations in this critically ill population of children.

NCT ID: NCT01089400 Completed - Influenza Clinical Trials

Immuno-virological Characterization of Severe H1N1v Influenza Infection in Bronchoalveolar Lavage

FluBAL
Start date: October 2009
Phase: N/A
Study type: Observational

The influenza A/H1N1v pandemic virus causes severe pneumonia that can lead to acute respiratory distress syndrome and death even in healthy young individuals. The respective roles of viral replication, bacterial infection and immune alterations of the host during such severe influenza H1N1v infection need to be clarified in order to optimize patients care. In this context, we aim to study immune and virological parameters in bronchoalveolar lavage fluid during severe influenza A/H1N1v infection with pulmonary involvement in intensive care unit. Results will be correlated to bacterial or viral pulmonary co-infections and to peripheral blood immune and virological parameters.

NCT ID: NCT01078831 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Intrabronchial Airway Pressures in Intubated Patients During Bronchoscopy

Start date: March 2002
Phase: N/A
Study type: Observational

The purpose of this study is to examine changes in ventilation and airway pressures during conventional bronchoscopy of intubated patients.