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comparing two method of respiratory support after surfactant administratio

Phase 2
Conditions
respiratory distress syndrome.
Respiratory distress of newborn
Registration Number
IRCT201308283915N9
Lead Sponsor
Research Vice Chancellor of Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
80
Inclusion Criteria

preterm infants with gestation age 30-35 weeks; admission in NICU with respiratory distress; treatment with surfactant
Exclusion criteria: preterm infants with gestation age less than 30 week or above 35 week; intubation immediately after birth before surfactant therapy; respiratory distress score more than 8; severe respiratory distress syndrome in chest x ray.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
eed for intubation in first 72 hours. Timepoint: every hour till 2 hours. Method of measurement: clinical assessment.
Secondary Outcome Measures
NameTimeMethod
Bronchopulmonary dysplasia. Timepoint: daily till 28 days. Method of measurement: clinically by supplementary oxygen reception.;Duration of hospitalization. Timepoint: daily till discharge. Method of measurement: medical records.
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