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

Not Applicable

Recruiting

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

• Registration Number: IRCT20150423021910N8
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 8 March 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 196

Inclusion Criteria

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

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of CPAP. Timepoint: Hour. Method of measurement: Questionnaire.

Secondary Outcome Measures

Name	Time	Method
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.