A comparative study of two surfactant administration techniques
Phase 2
- Conditions
- Health Condition 1: P220- Respiratory distress syndrome of newborn
- Registration Number
- CTRI/2024/01/061707
- Lead Sponsor
- School of Medical Sciences and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Preterm infants less than 36 weeks which are fulfilling the criteria for RDS and are spontaneously breathing
Exclusion Criteria
Preterm neonates with
Anatomical abnormalities of upper airway Congenital Diaphragmatic hernia
Choanal atresia
Trachea-oesophageal fistula
Cleft palate
- Requiring intubation with invasive ventilation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Efficacy of LISA technique over InSurETimepoint: At 12 hours, 72 hours, throughout the study time period
- Secondary Outcome Measures
Name Time Method eed for mechanical ventilationTimepoint: within 72 hours of birth;need for two or more doses of surfactantTimepoint: within 12 hours of birth