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Comparison of effectiveness of surfactant administration via endotracheal tube and thin endotracheal catheter in neonates with respiratory distress.

Phase 3
Recruiting
Conditions
Acute Respiratory Distress.
Respiratory distress syndrome of newborn
Registration Number
IRCT2017102110222N16
Lead Sponsor
Vice chancellor for research, Shahrekord University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
104
Inclusion Criteria

RDS clinical symptoms include respiratory distress; tachypnea.
Exclusion criteria: major anomalies; mother curioamniotic history; early sepsis; need to continue mechanical ventilation immediately after injection of surfactant.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Frequency of administration of surfactant. Timepoint: Twenty eight later. Method of measurement: checklist.
Secondary Outcome Measures
NameTimeMethod
Duration of oxygen demand. Timepoint: Twenty eight day later. Method of measurement: checklist.
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