Comparison of two different interfaces for delivering non-invasive ventilation in preterm neonates
Phase 2
- Conditions
- Health Condition 1: P228- Other respiratory distress of newbornHealth Condition 2: P220- Respiratory distress syndrome of newbornHealth Condition 3: P221- Transient tachypnea of newborn
- Registration Number
- CTRI/2023/07/055835
- Lead Sponsor
- Dr Deepak Chawla
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All inborn neonates admitted in NICU who fulfill the following criteria will be enrolled:
1.Gestation age at birth â?? 280/7 to 366/7 weeks
2.Receiving non-invasive positive pressure ventilation (NIPPV) for
1.A primary mode of respiratory support
2.Post- extubation respiratory support
3.Within 6 hours of initiation of NIPPV
4.Postnatal age <= 28 days
The neonate once randomized to the study group will remain allocated to that group for the first instance of respiratory support â?? for both the primary mode of respiratory support and for post-extubation support.
Exclusion Criteria
1.Major congenital malformations
2.Pulmonary air leaks at the time of enrolment
3.Refractory shock at the time of enrolment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method