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The effect of usual endotracheal tube replacement with endotracheal tube with capability of subglottic suction on reduction of ventilator associated pneumonia in patients

The effect of usual endotracheal tube replacement with endotracheal tube with capability of subglottic suction on reduction of ventilator associated pneumonia in patients admitted in adults intensive care units medical sciences

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201509266651N1
Enrollment
128
Registered
2016-04-25
Start date
2015-10-23
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

Pneumonia. Bacterial pneumonia, not elsewhere classified

Interventions

Intervention 1: Patients in the control group are under mechanical ventilation with conventional endotracheal tube (7 or 7.5 mm internal diameter for women and 8 or 8.5 mm for men). Intervention 2: In
Prevention
Patients in the control group are under mechanical ventilation with conventional endotracheal tube (7 or 7.5 mm internal diameter for women and 8 or 8.5 mm for men)
In the case group patients' previous tracheal tube to be replaced with tracheal tube with capability of subglottic suction (inner diameter of 7 or 5.7 mm for women or 8 or 8.5 mm for men).

Sponsors

Vice Chancellor for Research, Shiaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age over 18; patients with endotracheal tube in the ICU, mechanical ventilation for more than 48 hours, pneumonia before intubation and mechanical ventilation, cardiac disease. Exclusion criteria: immune deficiency, using immune system inhibitor drugs (cytotoxic chemotherapy or corticosteroids more than 160 mg hydrocortisone, prednisone 40 mg, 6 mg of dexamethasone or its equivalent; extubation less than 48 hours after intubation; death less than 48 hours after intubation, difficult intubation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ventilator associated pneumonia. Timepoint: DAILY. Method of measurement: 2015 GUIDLINE ,Centers for Disease Control(CDC).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Savaie

Shiraz University of Medical Sciences

savaie@sums.ac.ir+98 71 3647 4270

Outcome results

None listed

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