To assess pain and discomfort and use measures to decrease pain during surfactant administration in premature babies
Not Applicable
- Conditions
- Health Condition 1: P220- Respiratory distress syndrome of newborn
- Registration Number
- CTRI/2024/05/066746
- Lead Sponsor
- Department of Neonatology Government medical College Chh Sambhajinagar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All babies of GA less than 37 weeks with diagnosis of RDS requiring surfactant therapy with either LISA or INSURE methods.
Exclusion Criteria
1.Intubation before the study entry
2.Perinatal asphyxia
3.IVH more than grade II
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess Pain profile during surfactant therapy with either LISA or INSURE method in preterm neonates diagnosed with RDSTimepoint: 1 Before surfactant administration <br/ ><br>2 During laryngoscopy <br/ ><br>3 During surfactant administration <br/ ><br>4 After the procedure
- Secondary Outcome Measures
Name Time Method Adequacy of analgesiaTimepoint: During surfactant therapy