Search for Clinical Trial Results

Sponsored By

Respiratory Distress Syndrome, Infant - 20 Studies Found

Status Study
Terminated Study Name: Curosurf/Budesonide for Infants With Respiratory Distress Syndrome
Condition: Respiratory Distress Syndrome
Date: 2013-12-11
Interventions: Drug: Budesonide Experimental: Cursurf and Budesonide The baby with respiratory distress syndrome was gi
Recruiting Study Name: Tolerance of nHFPV Versus nCPAP in Neonatal Respiratory Distress
Condition: Neonatal Respiratory Distress
Date: 2014-01-07
Interventions:
  • Device: Nasal continuous airway positive pressure (nCPAP)
Not yet recruiting Study Name: Iloprost in Acute Respiratory Distress Syndrome
Condition: Respiratory Distress Syndrome, Adult
Date: 2017-04-06
Interventions:
  • Drug: Iloprost Iloprost nebuli
Not yet recruiting Study Name: Urine NT-ProBNP in Neonatal Respiratory Distress
Condition: Neonatal Respiratory Distress
Date: 2013-12-03
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: 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
Not yet recruiting Study Name: Repair of Acute Respiratory Distress Syndrome by Stromal Cell Administration (REALIST)
Condition: Acute Respiratory Distress Syndrome
Date: 2017-02-01
Interventions:
  • Biological: Human umbilical cord derived CD362 +ve MSCs

Completed Study Name: Comparison of Curosurf and Infasurf in the Treatment of Preterm Infants With Respiratory Distress Syndrome
Condition: Respiratory Distress Syndrome
Date: 2016-05-19
Interventions:
  • Drug: Poractant alfa Randomize
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
Active, not recruiting Study Name: Human Mesenchymal Stem Cells For Acute Respiratory Distress Syndrome (START)
Condition: Respiratory Distress Syndrome, Adult
Date: 2014-03-19
Interventions:
  • Biological: Allogeneic Bone Marrow-Derived Human Mesenchymal Stem Cells

Next >>>