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Acute Lung Injury clinical trials

View clinical trials related to Acute Lung Injury.

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NCT ID: NCT00399581 Completed - Clinical trials for Respiratory Distress Syndrome, Adult

Comparison of Two Methods of High Frequency Oscillatory Ventilation in Individuals With Acute Respiratory Distress Syndrome

Start date: November 2006
Phase: Phase 2
Study type: Interventional

Acute respiratory distress syndrome (ARDS) is a severe lung condition that causes respiratory failure. Individuals with ARDS often require the use of an artificial breathing machine, known as a mechanical ventilator. High frequency oscillatory ventilation (HFOV) is a form of mechanical ventilation that pumps small amounts of air into the lungs at a constant high rate. The purpose of this study is to compare the safety and efficacy of two HFOV methods in individuals with ARDS.

NCT ID: NCT00357929 Terminated - Clinical trials for Respiratory Distress Syndrome, Adult

Weaning From Mechanical Ventilation Using Permissive Hypercarbia

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

Some patients receiving mechanical ventilation have difficulty weaning off the ventilator because of physiological factors such as pre-existing lung disease, respiratory distress syndrome, and trauma among others. Allowing patients to become hypercarbic (increased blood bicarbonate level) may make it easier for these patients to be taken off the ventilator and resume breathing on their own.

NCT ID: NCT00351533 Completed - Clinical trials for Acute Respiratory Distress Syndrome

A Phase II Randomized Trial of Fish Oil in Patients With Acute Lung Injury (ALI)

Start date: July 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether fish oil (containing omega-3 fatty acids) given enterally is safe and effective in reducing lung and systemic inflammation seen in acute lung injury.

NCT ID: NCT00343993 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Noninvasive Positive Pressure Ventilation for ALI/ARDS:a Multicentre Randomized Controlled Trial

Start date: June 2006
Phase: Phase 1
Study type: Interventional

with appropriate inspired oxygen concentrations, NPPV would prevent intubation and hence avert the poor outcome associated with the need of invasive ventilation in patients with ALI/ARDS.

NCT ID: NCT00319631 Withdrawn - Clinical trials for Respiratory Distress Syndrome, Adult

Role of Vascular Endothelial Growth Factor (VEGF) in Acute Lung Injury/Adult Respiratory Distress Syndrome (ARDS)

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

Understanding the role VEGF plays in ARDS consequently provides an ideal opportunity to discover new therapies for ARDS.

NCT ID: NCT00314548 Completed - Clinical trials for Pulmonary Hypertension

Inhaled Prostacyclin for Adult Respiratory Distress Syndrome (ARDS) and Pulmonary Hypertension

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

Summary of the proposed research: The intravenous application of prostacyclin (PGE1) or its stable analogue, iloprost, has been used to cause a decrease not only of the pulmonary but also of the systemic vascular tone. Aerosolized prostacyclin, on the other hand, can result in a selective pulmonary vasodilatation without affecting the systemic blood pressure as shown in preliminary studies/case reports. No large trials exist for this type of use of the drug so far. Furthermore, aerosolized PGI2 can improve gas exchange and pulmonary shunt in clinical settings of impaired ventilation/perfusion ratio as it occurs in adult respiratory distress syndrome (ARDS) due to the redistribution of pulmonary blood flow from non-ventilated to ventilated, aerosol accessible lung regions. Therefore, the investigators propose to carry out a prospective, double blinded, randomized trial to show that the nebulized iloprost decreases pulmonary hypertension selectively and improves oxygenation in ARDS.

NCT ID: NCT00308022 Withdrawn - Pneumonia Clinical Trials

Comparison Study of High Frequency Percussive Ventilation With Conventional Ventilation

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

This study is designed to exam the effects of early management with high frequency percussive ventilation (HFPV) on patients with lung injury. Patients at risk for Acute Respiratory Distress Syndrome (ARDS) will be enrolled and randomized to one of two groups. One group will be managed with HFPV. The second group will be managed with conventional ventilation utilizing lung protective techniques. The primary endpoint of the study is rate of ventilator associated pneumonia. We hypothesized that use of HFPV in patients at risk for the development of ARDS will decrease the rate of ventilator associated pneumonia when compared to patients managed with conventional ventilation.

NCT ID: NCT00300248 Completed - Clinical trials for Respiratory Distress Syndrome, Adult

Long-Term Results in Mechanically Ventilated Individuals With Acute Lung Injury/Acute Respiratory Distress Syndrome

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

Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) is a severe lung condition that causes respiratory failure. Individuals with ALI/ARDS often require the use of a respirator or artificial breathing machine, known as a mechanical ventilator, while in an intensive care unit (ICU). Past research has shown that improved short-term clinical outcomes result from the use of a protective mechanical ventilation technique for the lungs. This study will evaluate the effects of lower tidal volume ventilation, and other aspects of critical illness and ICU care, on the long-term clinical outcomes of individuals with ALI/ARDS.

NCT ID: NCT00295269 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Corticosteroids as Rescue Therapy for the Late Phase of Acute Respiratory Distress Syndrome

Start date: March 1997
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess innovative treatment methods in patients with adult respiratory distress syndrome (ARDS) as well as those at risk of developing ARDS.

NCT ID: NCT00290602 Completed - Clinical trials for Postoperative Complications

Early Low Dose Steroid Therapy of Acute Respiratory Distress Syndrome

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the 2mg/kg administration of corticosteroids, in the form of methylprednisolone sodium succinate, in early phase acute respiratory distress syndrome after thoracic surgery, will reduce the postoperative mortality.