Investigation of the effects of nebulized ventolin and saline .%9 in transient respiratory distress of newbor
Phase 1
- Conditions
- Transient tachypnoea of newborn.Transient tachypnoea of newborn
- Registration Number
- IRCT2016010225811N1
- Lead Sponsor
- Vice chancellor for research,Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Term/near term neonates with transient tachypnea of newborn; without Sepsis; pneumonia; congenital heart disease; Pulmonary hypertension. Exclusion criteria: Preterm neonates with Respiratory distress syndrome; pneumonia; sepsis; surfactant requirement.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Admission durations. Timepoint: during study and drug injection every 6 hour. Method of measurement: days.;CPAC application hours. Timepoint: primary 24 hours. Method of measurement: hour.;Mechanical ventilation application hours. Timepoint: primary 24 hours. Method of measurement: hour.
- Secondary Outcome Measures
Name Time Method Arrhymia. Timepoint: during study. Method of measurement: cardiac monitor.