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Heated Humidified High Flow Nasal Cannula and RDS recovery in newborns

Not Applicable
Conditions
ewborn RDS.
Respiratory distress of newborn
Registration Number
IRCT2012092410430N3
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

Newborns receiving surfactant due to affiliation with RDS and their oxygen saturation was equal or more than 90% under nCPAP with CDP=4 cm H2O and FiO2<30% during the last 4 hrs, who still needed oxygen supplement after disconnection from nCPAP were included in the study; the exclusion criteria for this study were if there was a congenital malformation; prenatal asphyxia (min 5 apgar score equals 0 to 3, or umbilical cord pH less than 7, and the Bicarbonate level of the umbilical cord was reported to be less than 12), or nasal mucosa erythematic.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Humidity. Timepoint: Every 6 hours. Method of measurement: Hygrometer.
Secondary Outcome Measures
NameTimeMethod
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