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Efficacy of continuous positive airway pressure (CPAP) administration in delivery room for neonates with respiratory distress

Outcome of continuous positive airway pressure (CPAP) administration in delivery room for neonates with respiratory distress: a randomised control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/043888
Enrollment
130
Registered
2022-07-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J989- Respiratory disorder, unspecified

Interventions

Intervention1: 1-Free flow oxygen by face mask : 1-Free flow oxygen by face mask Duration : Settling of respiratory distress / 1 hour whichever is earlier Control Intervention1: Continuous positive ai

Sponsors

Tanmay Marathe
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Neonates delivered with gestational age >35 weeks by normal vaginal delivery/LSCS and develop laboured breathing in the delivery room or require free flow oxygen to maintain SPO2 in target range.

Exclusion criteria

Exclusion criteria: 1-Neonates with gestation 2-Neonates with antenatally or immediate postnatally detected life threatening congenital anomalies 3-Neonates needing prolonged PPV or intubation as per NRP algorithm

Design outcomes

Primary

MeasureTime frame
Outcome of delivery room CPAP in reducing the severity and duration of respiratory distressTimepoint: Status of respiratory distress at 1 hour of life—

Secondary

MeasureTime frame
Outcome of delivery room CPAP on NICU admissions and the early neonatal outcomeTimepoint: 1 year—

Countries

India

Contacts

Public ContactTanmay Marathe

Jawaharlal Nehru Medical College,KAHER University ,Belagavi

manisha.bhandankar1970@gmail.com08793714445

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026