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The effect of expiratory rib cage compression before endotracheal suctioning on hemodynamic changes

The effect of expiratory rib cage compression before endotracheal suctioning on hemodynamic changes in mechanically ventilated patients in ICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016021326537N1
Enrollment
58
Registered
2016-05-12
Start date
2016-05-21
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

Mechanically ventilated patients. Diseases of the respiratory system

Interventions

Intervention 1: In intervention group use expiratory ribcage compression befor suctioning .Then standard suction is done during three times a day. Intervention 2: In control group suctioning without r
Prevention
In intervention group use expiratory ribcage compression befor suctioning .Then standard suction is done during three times a day
In control group suctioning without rib cage compression is done

Sponsors

Vice chancellor for Research of Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Iclusionl criteria: age 18 to 65 years, having endotracheal tube for 24 hour, stable hemodynamic status (mean arterial pressure between 110 to 60 mm Hg, heart rate of less than 110 beats per minute), lack of a chest tube, no chest surgery or injuries, no rib fractures, no skin grafts and reconstructive surgery of the chest,no pregnancy, obesity (body mass index (BMI)> 30) Exclusion criteria: mucolytic and muscle paralysis drugs, start, stop, or change the bronchodilator medications during the study, extubation during the study period, using paralyze anesthesia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood pressure. Timepoint: Bp will be measured three times: five minutes prior to the endotracheal suctioning, and 15 and 25 minutes following the procedure. Method of measurement: using of the Sphygmomanometer.;O2 Saturation. Timepoint: SpO2 will be measured three times: five minutes prior to the endotracheal suctioning, and 15 and 25 minutes following the procedure. Method of measurement: with pulse Oximetry (Monitor observation).;Heart Rate. Timepoint: HR will be measured three times: five minutes prior to the endotracheal suctioning, and 15 and 25 minutes following the procedure. Method of measurement: Via monitor observation.

Secondary

MeasureTime frame
Respiratory Rate. Timepoint: Respiratory rate will be measured three times:five minutes prior to the endotracheal suctioning, and 15 and 25 minutes following the procedure. Method of measurement: Counting the respiratory rate of the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Yaghoubi

Ahvaz University of Medical Sciences

m4ry4myaghoubi@gmail.com+98 84 3223 1523

Outcome results

None listed

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