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Effect of Position on duration of respiratory support in Premature newborns with RDS receiving NCPAP

Comparison of the Effect of Supine and Prone Position on duration of respiratory support in Premature newborns with RDS receiving NCPAP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150423021910N6
Enrollment
136
Registered
2020-10-18
Start date
2018-09-23
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

Respiratory Distress Syndrom. Respiratory distress syndrome of newborn

Interventions

Intervention 1: Intervention group: The newborns in case group put in prone position and only for feeding and nurse care position change to supine for maximum 15 minute. respiratory support was establ
at first CDP equal to 6-8 cmH2O and Fio2=30% was administrated. In case, the newborn needed inspiratory oxygen fraction of higher than 40% to maintain oxygen saturation in the right hand at 90–95% for

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 30 to 34 W Affiliated from RDS Mother received one course of steroid therapy before delivery

Exclusion criteria

Exclusion criteria: Lack of Congenital Heart Disease Lack of Defects interfere with specific position Lack of Perinatal Asphyxia Lack 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.;Time to full enteral feeding. Timepoint: During study. Method of measurement: Clinical examination.;The number of surfactant administration. 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 3386 8247

Outcome results

None listed

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