Comparing the effectiveness of two mask and nasal tube ventilation methods in premature infants with respiratory failure
Phase 3
- Conditions
- Respiratory distress syndrome of newborn.Respiratory distress syndrome of newborn
- Registration Number
- IRCT2017050517413N25
- Lead Sponsor
- Vice Chancellor for Research, Baqiyatallah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
gestational ages of less than 34 weeks ; birthweight of less than 1800 gr; respiratory distress despite receiving Surfactant and mechanical ventilation; needed FIO2 of less than 60% after extubation
Exclusion criteria:anomalies in nasopharyngeal path, heart or lungs; chromosomal anomalies; intraventricular hemorrhage (IVH); not willing to participate
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of ventilation. Timepoint: After intervention. Method of measurement: Time record by nurse.;Oxygen Saturation. Timepoint: After intervention. Method of measurement: Pulse Oxymetry.;Arterial oxygen pressure. Timepoint: After intervention. Method of measurement: Arterial Blood Gas Assessment.;Respiratory rate. Timepoint: After intervention. Method of measurement: one minute counting by nurse.
- Secondary Outcome Measures
Name Time Method Abdominal Distention. Timepoint: After intervention. Method of measurement: Physical examination.;Mortality. Timepoint: After intervention. Method of measurement: Recording mortality cases.;Intraventricular hemorrhage. Timepoint: After intervention. Method of measurement: Brain sonography.;Necrotizing Enterocolitis. Timepoint: After intervention. Method of measurement: Physical examination.