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The efficacy of nasal high frequency ventilation in treatment of neonatal respiratory syndrome

Not Applicable
Recruiting
Conditions
Respiratory distress syndrome.
Respiratory distress syndrome of newborn
Registration Number
IRCT2017062734782N1
Lead Sponsor
Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
62
Inclusion Criteria

premature and term neonate; more than 1000 gram and 30 weeks of gestational age; spontaneous breathing; respiratory distress syndrome symptoms required treatment
Exclusion criteria: major congenital anomaly; diaphragmatic hernia; cyanotic heart disease; intrauterine growth retardation; asphyxia

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The duration of non-invasive support. Timepoint: Every hour. Method of measurement: hourly NICU recorded sheets.
Secondary Outcome Measures
NameTimeMethod
Pulmonary hemorrhage. Timepoint: hourly. Method of measurement: physical exam and chest xray if needed.;Narcotizing enterocolitis (NEC). Timepoint: Daily. Method of measurement: Daily recorded sheets and daily physical exam and abdominal xray if needed.;Intraventricular hemorrhage (IVH). Timepoint: at the 3rd and 7th days after birth. Method of measurement: brain sonography.;Respiratory failure and intubation. Timepoint: continuously every hour during non-invasive respiratory support. Method of measurement: NICU record sheets.;Pnuemothorax. Timepoint: continuously every hour during non-invasive respiratory support. Method of measurement: NICU record sheets.;Chronic lung disease. Timepoint: 4 weeks after birth. Method of measurement: NICU record sheets.;Patent ductus arteriosus. Timepoint: Daily physical exam. Method of measurement: Daily recorded sheets.;Time to full enteral feeding. Timepoint: Daily till full feeding. Method of measurement: Daily recorded sheets.
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