Comparison of the effects of High flow nasal cannula versus nasal continuous positive Air way pressure in treatment of respiratory distress syndrome in premature newborns
Not Applicable
- Conditions
- Respiratory distress syndrome.Respiratory distress syndrome of newborn
- Registration Number
- IRCT2015100814333N41
- Lead Sponsor
- Vice chancellor for research, Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
premature infants under 37 weeks and over 24 weeks; respiratory distress syndrome; written informed consent of the parents
Exclusion criteria: Apgar score of fifth minute less than 5; there are syndromes or major congenital anomalies; congenital heart disease, mother Radiography and chorioamnionitis
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cerebral hemorrhage. Timepoint: During study. Method of measurement: By cerebral ultrasound.;Necrotizing enterocolitis. Timepoint: During study. Method of measurement: Based on the clinical symptoms and a doctor observation and an abdominal radiograph.;Amount of nasal septum injury. Timepoint: During study. Method of measurement: Based on the doctor examination.;Air leak syndrome. Timepoint: During study. Method of measurement: Based on the clinical symptoms and doctor observation and chest radiography.;Broncho-pulmonary dysplasia. Timepoint: During study. Method of measurement: Based on the clinical symptoms, doctor observation, x-ray and laboratory.;The need for re-intubating. Timepoint: During study. Method of measurement: Based on laboratory and doctor clinical examination.
- Secondary Outcome Measures
Name Time Method