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Evaluation of appropriate for delivering positive expiratory pressure in preterm newborns affiliated from RDS

Comparison the effect of nasal mask and nasal prong on duration of nasal CPAP support and other complications of prematurity in preterm newborns affiliated from RDS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150423021910N8
Enrollment
196
Registered
2022-02-11
Start date
2022-02-20
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Respiratory Distress Syndrome. Respiratory distress syndrome of newborn

Interventions

Intervention 1: Intervention group: The newborns in first group put in supine position and respiratory support was established with nCPAP (Bubble CPAP Infant Delivery System, Fisher & Paykel, Auckland
at first CDP equal to 6-8 cmH2O and Fio2=30% was administrated. If the newborn needed inspiratory oxygen fraction of higher than 40% to maintain oxygen saturation in the right hand at 90–95% for more

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 30 Days

Inclusion criteria

Inclusion criteria: Gestational age between 28 to 34 W Affiliated from RDS Mother received one course of steroid therapy before delivery

Exclusion criteria

Exclusion criteria: Existence of Congenital Heart Disease Existence of Perinatal Asphyxia(umbilical pH less than 7/2 and bicarbonate less than 12) Existence of maternal chorioamnionitis

Design outcomes

Primary

MeasureTime frame
Duration of CPAP. Timepoint: Hour. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Mean of CPAP. Timepoint: During study. Method of measurement: CPAP desktop.;Duration of hospitalization. Timepoint: Daily. Method of measurement: Questionnaire.;Need for mechanical ventilation. Timepoint: During study. Method of measurement: Clinical examination.;Bronchopulmonary dysplasia. Timepoint: During study. Method of measurement: Clinical examination.;Pneumothorax. Timepoint: During study. Method of measurement: Chest X ray.;The number of surfactant administration. Timepoint: During study. Method of measurement: Clinical examination.;Nasal trauma. Timepoint: During study. Method of measurement: Clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehzad Barekatain

Esfahan University of Medical Sciences

b_barekatain@med.mui.ac.ir+98 31 3261 6670

Outcome results

None listed

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