Respiratory Distress Syndrome.
Conditions
Interventions
Intervention group 1: In infants that are under nasal continuous positive airway pressure and ventilator, gradually flow continues increase to CDP = 6 inches, H2O and FiO2 = 30%. A requirement of FiO2
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
All
Age
1 Days to 14 Days
Inclusion criteria
Inclusion criteria: Infants that have clinical signs of respiratory distress syndrome. Infants that their ages are have 2 weeks. Infants receiving nasal continuous positive airway pressure with surfactant.
Exclusion criteria
Exclusion criteria: Infants that have congenital anomalies. Infants that have perinatal asphyxia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of infants with respiratory distress syndrome. Timepoint: Before the intervention and every 12 hours after the administration of surfactant in the intervention group and surfactant with budosonide 0.25 mg intratracheally in the control group. Method of measurement: Mechanical Ventilation Device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction of respiratory distress syndrome in preterm infants prescribed with surfactant and surfactant with budesonide. Timepoint: Before the intervention and every 12 hours after the administration of surfactant in the intervention group and surfactant with budosonide 0.25 mg intratracheally in the control group. Method of measurement: Mechanical Ventilation Devices. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Tohidnia
Qazvin University of Medical Sciences
Outcome results
None listed