Study comparing two different techniques of surfactant administration in preterm babies with respiratory distress syndrome
Not Applicable
- Conditions
- Health Condition 1: P220- Respiratory distress syndrome of newborn
- Registration Number
- CTRI/2020/05/025360
- Lead Sponsor
- Department of Neonatology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All criteria to be full filled-
-Inborn preterm infant 26 weeks to 34 weeks of gestational age
-Infants with typical sign and symptoms of RDS
-Infants require nCPAP treatment with required fraction of inspired oxygen (FiO2)-0.4 or more in first 6 hours of life.
Exclusion Criteria
Anyone of the following-
-Infants with major congenital anomalies.
-Severe birth asphyxia, Apgar score <4 and cord Ph < 7.0
-Required intubation in birthing area prior to first surfactant dose
-Shock prior to randomization
-No parental consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method