Comparison of endotracheal tube and thin catheter for surfactant therapy in neonates with respiratory distress syndrome

Phase 3

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

• Registration Number: IRCT20211006052685N2
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Infants born with a gestational age of 25 to 37 weeksA
dmitted to the NIC

Exclusion Criteria

Respiratory distress due to cardiac causes
hemodynamic instability
sepsis and any cause other than surfactant deficiency

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Treatment of respiratory distress syndrome. Timepoint: Evaluate respiratory condition of neonates at birth up to 30 days after birth. Method of measurement: Evaluate the duration and amount of need for mechanical ventilation, NCPAP and FiO2.