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Effect of endotracheal suctioning on clinical outcomes in preterm neonates

Comparison of two methods open and closed endotracheal suctioning on clinical outcomes in preterm neonates in NICUs of Alzahra and Taleghani Teaching Hospitals, Tabriz, 2012

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204078315N3
Enrollment
90
Registered
2012-05-13
Start date
2012-05-14
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Evaluation of suction effect. Respiratory conditions due to unspecified external agent

Interventions

Intervention 1: In closed group tracheal sactioning will be continued for atlleast48 huors. BP,HR,O2SAT should be recorded one minute before and one and five minutes after procedure,How ever frequency
Treatment - Other
In closed group tracheal sactioning will be continued for atlleast48 huors. BP,HR,O2SAT should be recorded one minute before and one and five minutes after procedure,How ever frequency of suctioning a
In open group tracheal sactioning will be continued for atlleast48 huors. BP,HR,O2SAT should be recorded one minute before and one and five minutes after procedure,How ever frequency of suctioning an

Sponsors

Research Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 10 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactrahele janani

Tabriz University of Medical Sciences

rahele_janani@yahoo.com+98 41 1328 0465

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026