Status | Study |
Completed |
Study Name: Human Mesenchymal Stem Cells For Acute Respiratory Distress Syndrome Condition: Acute Respiratory Distress Syndrome Date: 2013-01-18 Interventions: Biological: Allogeneic Bone Marrow-Derived Human Mesenchymal Stem Cells Allogeneic Bone Marrow-Derived H |
Recruiting |
Study Name: Efficacy Study of Dexamethasone to Treat the Acute Respiratory Distress Syndrome Condition: Acute Respiratory Distress Syndrome Date: 2012-11-18 Interventions: Drug: Dexamethasone Dexamethasone (20 mg/iv/daily/from Day 1 of randomization during 5 days, followed by |
Completed |
Study Name: Effects of Positive End-expiratory Pressure and Tidal Volume on Fluid Responsiveness of Acute Respiratory Distress Syndrome Condition: Respiratory Distress Syndrome, Adult Date: 2012-10-26 Interventions: Other: Infusion of 6% tetrastarch for a total of 500 ml |
Completed |
Study Name: First In Human Study on Synthetic Surfactant CHF 5633 in Respiratory Distress Syndrome Condition: Respiratory Distress Syndrome in Premature Infants Date: 2012-04-20 Interventions: Drug: synthetic surfactant (CHF5633) CHF5633 100 mg/kg; CHF5633 200 mg/kg synthetic surfactant sterile s |
Terminated |
Study Name: High Frequency Oscillatory Ventilation for Acute Respiratory Distress Syndrome (ARDS) Condition: Acute Respiratory Distress Syndrome Date: 2011-11-21 Interventions: Device: Lung protective CMV Lo |
Completed |
Study Name: Serial Changes of Soluble Triggering Receptor Expressed on Myeloid Cells-1 (sTREM-1) Levels in Patients With Acute Respiratory Distress Syndrome Condition: Acute Respiratory Distress Syndrome Date: 2007-11-12 |
Completed |
Study Name: Effect of Prone Positioning on Mortality in Patients With Severe and Persistent Acute Respiratory Distress Syndrome Condition: Acute Respiratory Distress Syndrome Date: 2007-09-10 Interventions: Procedure: prone position prone position for at least 16 hours per day |
Withdrawn |
Study Name: Role of Vascular Endothelial Growth Factor (VEGF) in Acute Lung Injury/Adult Respiratory Distress Syndrome (ARDS) Condition: Respiratory Distress Syndrome, Adult Date: 2006-04-27 |
Completed |
Study Name: Delivery Room Management Trial of Premature Infants at High Risk of Respiratory Distress Syndrome Condition: Respiratory Distress Syndrome, Newborn Date: 2005-10-24 Interventions: Drug: PS Group Intubation, pro |
Completed |
Study Name: Nitric Oxide Administration for Acute Respiratory Distress Syndrome Condition: Acute Respiratory Distress Syndrome Date: 2005-10-14 Interventions: Drug: Nitric Oxide Subjects wi |