Administration of surfactant by thin catheter (LISA) using video laryngoscope to decrease pain in neonates
Phase 2
Recruiting
- Conditions
- Health Condition 1: P220- Respiratory distress syndrome of newborn
- Registration Number
- CTRI/2022/09/045204
- Lead Sponsor
- Mude Praneetha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Preterm neonates requiring rescue surfactant, i.e., FiO2 requirement > 0.3 on CPAP pressure of at least 6 cm H2O
Exclusion Criteria
Neonates who require intubation in the delivery room for stabilization
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method FANS score (Faceless acute neonatal pain scale) will be assessed to evaluate procedural pain in neonates below 35 weeks of gestational age while administering surfactant by LISA technique using any of the two laryngoscopes (video vs. conventional)Timepoint: 1. 5 minutes before procedure (baseline) <br/ ><br>2. Immediately post procedure <br/ ><br>3. 5 minutes post procedure <br/ ><br>4. 10 minutes post procedure
- Secondary Outcome Measures
Name Time Method Incidence of intraventricular hemorrhageTimepoint: on day 7 of life;Number of attempts to complete the procedure successfullyTimepoint: At the time of procedure;Time taken to complete <br/ ><br>the procedure <br/ ><br>Timepoint: At the time of procedure;To record adverse events during the procedureTimepoint: At the time of procedure