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The effects of routine versus a minimally invasive endotracheal tube suctioning procedure on suction-related pain, airway clearance, airway trauma and physiological indices in patients hospitalized in intensive care units of Al-Zahra Hospital of Isfahan in 2015.

Comparison the effects of routine versus a minimally invasive endotracheal suctioning

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015072423314N1
Enrollment
60
Registered
2015-08-12
Start date
2015-08-10
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 conditions due to other specified external agents. Respiratory conditions due to other specified external agents

Interventions

Intervention 1: In intervention group (minimally invasive endotracheal tube suctioning) the patients were hyper oxygenated only by ventilator for one minute, short suction catheter with effective leng
Treatment - Other
In intervention group (minimally invasive endotracheal tube suctioning) the patients were hyper oxygenated only by ventilator for one minute, short suction catheter with effective length was introduce
In control group (routin endotracheal tube suctioning) after disconnecting the patients from the ventilator, manual hyper oxygenation and hyperventilation was carried out for one minute, a suction cat

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Major inclusion criteria: age over than 18; obtaining informed consent; no blood clotting disorders; no chronic respiratory disease; intubation time between 48 hours and one week. Major exclusion criteria: extubation during the study; become unstable hemodynamic parameters such as bradycardia, arrhythmia, cyanosis, loss of arterial oxygen.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Immediately before, immediately after, and 10 min after endotracheal suctioning. Method of measurement: With numeral rating scale (NRS).

Secondary

MeasureTime frame
Blood pressure. Timepoint: Immediately before, immediately after, and 10 min after endotracheal suctioning. Method of measurement: With vital signs monitoring devices.;Heart Rate. Timepoint: Immediately before, immediately after, and 10 min after endotracheal suctioning. Method of measurement: With vital signs monitoring devices.;Respiratory Rate. Timepoint: Immediately before, immediately after, and 10 min after endotracheal suctioning. Method of measurement: With vital signs monitoring devices.;Spo2. Timepoint: Immediately before, immediately after, and 10 min after endotracheal suctioning. Method of measurement: With vital signs monitoring devices.;Number of endotracheal suctioning. Timepoint: After each endotracheal suctioning. Method of measurement: Counting the number of endotracheal suctioning.;Airway traumatization. Timepoint: After endotracheal suctioning. Method of measurement: Viewing bleeding in the airways.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Shamali

Isfahan University of Medical sciences

gezaltoshmal@yahoo.com+98 31 3792 2917

Outcome results

None listed

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