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weaning from nasal continuous positive airway pressure in preterm infants

Comparing sudden Complete and gradual weaning on successful weaning from nasal CPAP in preterm infants

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180915041040N1
Enrollment
60
Registered
2018-11-30
Start date
2014-11-03
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Respiratory distress syndrome of newborn. Respiratory distress of newborn

Interventions

Intervention 1: Intervention group: infant is separated from NCPAP and is allowed to breathe in the room air with FiO2 of 21% or with extra oxygen with FiO2 of 40% for 4 hours. Then, NCPAP with 5 cm H

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 30 Days

Inclusion criteria

Inclusion criteria: Gestational age equal to or less than 32 weeks and birth weight equal to or less than 1800 gr Starting NCPAP from first hours of birth to treat respiratory distress syndrome Treatment with NCPAP after weaning from positive pressure ventilation via endotracheal route The newborn should be under treatment with NCPAP for at least 24 hours 5th minute APGAR score above 4

Exclusion criteria

Exclusion criteria: Documented congenital heart anomalies (except for small atrial septal defect, patent foramen ovale, and patent ductus arteriosus (PDA)) definite or possible neuromuscular disease definite or possible syndrome need for surgery transfer to other hospital patients weighing less than 750 g at the time of randomization intraventricular hemorrhage (grade above 2) lung hypoplasia other life-threatening congenital anomalies thoracic or airway anomalies need for mechanical ventilation before NCPAP removal

Design outcomes

Primary

MeasureTime frame
Successful NCPAP weaning in the first attempt. Timepoint: After first attempt to NCPAP weaning. Method of measurement: Number of attempts.

Secondary

MeasureTime frame
The frequency of weaning. Timepoint: After each time of weaning from the device. Method of measurement: Document.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoya Choopani

Esfahan University of Medical Sciences

choopani.r@skums.ac.ir+98 31 3792 7653

Outcome results

None listed

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