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The effect of normal saline in endotracheal suctioning on ventilation

The effect of endotracheal suctioning with and without normal saline on respiratory physiologic parameters in open heart surgery patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201008084531N1
Enrollment
40
Registered
2010-10-23
Start date
2010-07-16
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

Respiratory dysfunction. Other complications of procedures, not elsewhere classified

Interventions

Intervention 1: endotracheal suctioning with normal saline. Intervention 2: endotracheal suctioning without normal saline.
endotracheal suctioning with normal saline
endotracheal suctioning without normal saline

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: elective coronary artery bypass graft, age less than 65, normal pre-operative pulmonary function tests, no chronic obstructive pulmonary disease, normal arterial blood gases in room air and before induction , Ejection fraction more than 40%, stable hemodynamic status after transmission to ICU, normal arterial blood gases after transmission to ICU, under ventilation by bennet 760 Exclusion criteria: abnormal arterial blood gases, hemodynamic disturbance, smoking

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Arterial blood gases. Timepoint: one minute before and one, 5 and 15 minutes after the procedure. Method of measurement: arterial blood gases analysis.;End tidal CO2. Timepoint: one minute before and one, 5 and 15 minutes after the procedure. Method of measurement: by capnograph.;O2 saturation. Timepoint: one minute before and one, 5 and 15 minutes after the procedure. Method of measurement: by pulsoxymeter.;Peak inspiratory pressure, plateau pressure, dynamic compliance, static compliance and airway resistance. Timepoint: one minute before and one, 5 and 15 minutes after the procedure. Method of measurement: by monitoring of ventilator.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Akbar Visi Raygani

Kermanshah University of Medical Sciences

avisi@kums.ac.ir+98 83 1828 2102

Outcome results

None listed

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