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

Not Applicable

• Conditions: P22.0; Respiratory distress syndrome of newborn; eonatal respiratory distress syndrome.

• Registration Number: IRCT20201222049795N1
• Lead Sponsor: Semnan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

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

Exclusion Criteria

Patients with congenital anomalies
Patients needed endotracheal intubation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.