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?Assessing the effect of an oral hygiene protocol on ventilator associated pneumonia among the intubated patients hospitalized in Intensive care units

?Assessing the effect of an oral hygiene protocol on ventilator associated pneumonia among the intubated patients hospitalized in Intensive care units

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220215054026N1
Enrollment
200
Registered
2022-12-17
Start date
2016-06-01
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Ventilator associated pneumonia. Ventilator associated pneumonia

Interventions

Intervention 1: For the intervention group, in addition to all standard oral care, a supervised implementation of oral health guideline, including seven items will be considered as follows: 1) Wash yo

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age >=18 years Patient with no oral trauma Patient with no fracture in the face The patient must be intubated within the first 24 hours of admission. The patient has not been admitted to any other hospital department in the last 48 hours. Patients who are intubated for at least 1 week and at most 3 months. Written informed consent of the patient's guardian or companion (father, brother, grandfather) to participate in the study

Exclusion criteria

Exclusion criteria: Observing any injuries in the oral during the study Observinng any facial fracture during the study Patients who can remove the tracheal tube in less than 48 hours. Critically ill patients with life expectancy less than 48 hours

Design outcomes

Primary

MeasureTime frame
The occurence of ventilator-associated pneumonia (VAP). Timepoint: After 48 hours of intubation and doing intervention, each patient will be evaluated daily for the occurrence of ventilator-associated pneumonia. Method of measurement: Clinical criteria, the clinical pulmonary infection score (CPIS), that described initially by Johanson et al. And suggested by the Centers for Disease Control and Prevention (CDC), will be used to assess the VAP. This tool consists of clinical, microbiological, physiological and radiographic evidence and allow us a numerical value to predict the presence/absence of VAP .

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSharare Karimi

Sanandaj University of Medical Sciences

dr.karimi.sh@gmail.com+98 87 3366 4645

Outcome results

None listed

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