High flow nasal cannulae versus nasal continuous posituve airway pressure in neonates with Respiratory distress syndrome.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Preterm neonates
- Registration Number
- CTRI/2017/09/009910
- Lead Sponsor
- aveena Dias
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 84
Inclusion Criteria
all the preterm neonates less than 36weeks and downe score of more than 3.
Exclusion Criteria
1.Neonates with congenital cyanotic heart disease.
2.Neonates with major congenital malformations.
3.Neonates with air leak syndromes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Failure of non invasive respiratory support requiring invasive ventilation support with 72 hours of initiation of therapy.Timepoint: 1.Requiring invasive ventilation support with 72 hours of initiation of therapy.
- Secondary Outcome Measures
Name Time Method Days on Non-invasive support(CPAP/HFNC) days on Ventilator <br/ ><br>Days on Oxygen supplementation <br/ ><br>Days on Non-invasive support(CPAP/HFNC) days on Ventilator <br/ ><br>Days on Oxygen supplementation <br/ ><br>Nasal mucosal Injury <br/ ><br>Pneumothorax <br/ ><br>Abdominal distension <br/ ><br>Timepoint: 100