Effect of endotracheal suctioning on clinical outcomes in preterm neonates
Phase 1
- Conditions
- Evaluation of suction effect.Respiratory conditions due to unspecified external agent
- Registration Number
- IRCT201204078315N3
- Lead Sponsor
- Research Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
1- Preterm neonates of 27-34 weeks of gestational age born at Alzahra and Taleghani hospitals whom are admitted at NICU. 2- After maximum 24 hours of their admission to NICU are intubated due to the respiratory distress. 3- Neonates receiving surfactant. 4- Preterm neonates who are ventilated for at least 48 hours. 5- Neonates without congenital anomalies or heart diseases. 6- Neonates without MAS. 7- PROM less than 18 hours and 8- Neonates with less than 3 times of intubation trial.
Exclusion criteria: 1- Neonates with proved immune deficiency. 2- Neonates who are referred to other centers before completion of data and 3- Neonates whose congenital heart disease and ... is verified later.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Verification and comparison of physiological stability. Timepoint: Befor one minute and after one minute and after five minute. Method of measurement: By the use of Monitoring.;Number of suctioning needed. Timepoint: Duration of time from first suctioning till extubation. Method of measurement: Data record form.
- Secondary Outcome Measures
Name Time Method Duration of hospitalization. Timepoint: Untill discharch from NICU. Method of measurement: Data record form.;Side effects of suctioning. Timepoint: From 24 after first suctioning till extubation. Method of measurement: By use of data record form.