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A comparison of the effect of Nasal Continuous Positive Airway Pressure (NCPAP) vs Nasal high-frequency oscillation(NHFO) in the treatment of respiratory distress in preterm infants

A comparison of the effect of Nasal Continuous Positive Airway Pressure (NCPAP) vs Nasal high-frequency oscillation(NHFO) in the treatment of respiratory distress in preterm infants

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201222049795N1
Enrollment
20
Registered
2021-01-09
Start date
2020-09-30
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Neonatal respiratory distress syndrome. Respiratory distress syndrome of newborn

Interventions

Intervention 1: First intervention group: Nasal Continuous Positive Airway Pressure group
These infants underwent non-invasive ventilation Continuous Positive Airway Pressure using Bi nasal prong, Bubble Continuous Positive Airway Pressure, hot and humid airflow, and blender. Continuous Po

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Gestational age between 25 to 35 weeks Moderate to severe respiratory distress syndrome

Exclusion criteria

Exclusion criteria: Patients with congenital anomalies Patients needed endotracheal intubation

Design outcomes

Primary

MeasureTime frame
Preterm infants. Timepoint: Determining premature infants at the beginning of the study. Method of measurement: By measuring gestational age between 25 to 35 weeks.;Respiratory distress. Timepoint: At the beginning of the study. Method of measurement: Using medical examinations.

Secondary

MeasureTime frame
O2 Therapy. Timepoint: at any time interval of study If it's needed. Method of measurement: Using medical examinations.;O2 Therapy time. Timepoint: While O2 Therapy. Method of measurement: Counting the days of oxygen therapy.;Invasive mechanical ventilation. Timepoint: at any time interval of study If it's needed. Method of measurement: If the infant does not respond to non-invasive mechanical ventilation.;Duration of using mechanical ventilation. Timepoint: While using mechanical ventilation. Method of measurement: Counting the days of using mechanical ventilation and Using the data collection form.;The infant's age at the time of use of mechanical ventilation. Timepoint: While using mechanical ventilation. Method of measurement: Age is calculated based on hours and Using the data collection form.;Apnea. Timepoint: At any time of apnea During or after being placed under the studied devices. Method of measurement: By observing the infant's breathing measuring devices.;The infant's age at the time of apnea. Timepoint: At any time of apnea. Method of measurement: Age is calculated based on hours and Using the data collection form.;Surfactant. Timepoint: At any time of study if necessary. Method of measurement: Based on the physician's opinion and when there is no progress in the infant's respiratory recovery.;Age of infants at surfactant indication. Timepoint: At the time of surfactant indication. Method of measurement: Age is calculated based on hours and Using the data collection form.;Pneumothorax. Timepoint: During or after being placed under the studied devices. Method of measurement: By imaging and examination.;Age of infant's at the pneumothorax incidence. Timepoint: At the time of pneumothorax incidence. Method of measurement: Age is calculated based on hours and Using the data collection form.;IVH (Intra ventricular hemorrhage). Timepoint: During or after being placed under the studied devices. Method of measurement: imaging.;Age of infant's at intraventricul

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Jandaghi

Islamic Azad University

M.Jandaghi73@gmail.com+98 23 3332 3194

Outcome results

None listed

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