Evaluation of the effect of Beraksurf and Cursorf in patients with respiratory distress
Phase 3
Recruiting
- Conditions
- P22.0respiratory distress syndrome.Respiratory distress syndrome of newborn
- Registration Number
- IRCT20120126008827N3
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Gestational age < 37 weeks
Radiologic and clinical diagnosis during first 6 hours,
Need to Fio2>30% for keeping o2 saturation 92-95% that measured by pulse oximetry
Exclusion Criteria
Patients with congenital disease and anomalies
Receiving two types of surfactant due to lack or shortage of the drug
Patients need operation
Neonates with congenital heart or lung disease or abdominal pathology
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 and 2, 6,12,18,24,36,48 and 72 hour after birth. Method of measurement: Beraksurf case report form.
- Secondary Outcome Measures
Name Time Method