A comparative study of the response to Heated and Humidified High Flow Nasal Cannula treatment with Continuous Positive Airway Pressure method in premature infants with respiratory distress syndrome
Not Applicable
Recruiting
- Conditions
- Respiratory Distress Syndrome In Newborn.Respiratory distress syndrome of newbornP22.0
- Registration Number
- IRCT20231001059581N1
- Lead Sponsor
- Ghoum University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
RDS 4-6
Clinical sign Of RDS
Gestational Age Between 28 To 32
Weight Less Than 1500g
Exclusion Criteria
Major Congenital Anomaly
Asphyxia Sign
Cyanotic Heart Disease
Emergency Intubation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method RDS Score. Timepoint: From the beginning of the study, Every 4 hours until treatment or failure. Method of measurement: Downs scale Score.
- Secondary Outcome Measures
Name Time Method eed for intubation. Timepoint: Every 4 hours based on RDS score until treatment or failure. Method of measurement: Clinical examination, RDS score.;Treatment duration. Timepoint: Every 4 hours based on RDS score until treatment or failure. Method of measurement: Day.