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Oral Care to Prevent Ventilator-associated Pneumonia

Investigation of the Effect of Oral Care Given by Two Different Methods in Patients Connected to Mechanical Ventilators on the Development of Ventilator-AssociatedPneumonia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05161962
Enrollment
57
Registered
2021-12-17
Start date
2019-09-01
Completion date
2020-02-05
Last updated
2021-12-17

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

Conditions

Oral Hygiene, Oral Health, Ventilators, Mechanical

Keywords

Mechanical ventilation, nursing, oral care, pneumonia

Brief summary

This study was conducted to investigate the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.

Detailed description

The universe of this research, which was designed as a semi-experimental study, is composed of patients connected to the mechanical ventilator lying in Atatürk University Training and Research Hospital Anesthesia and Reanimation Intensive Care Unit between September 2019 and February 2020. A total of 57 patients, 29 method-1, 28 method-2 groups, met the inclusion criteria of the study. In the data collection phase, 'Patient Identifier Information Form', 'Patient Monitoring Form', 'Oral Assessment Scale' and 'Tracheal Aspirate Culture Result Form' were used. In the evaluation of the data, number and percentage distributions, Kruskal Wallis, Mann Withney-U, Wilcoxon Analysis, Chi-Square test were used.

Interventions

COMBINATION_PRODUCTOne group received standard oral care.

the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.

COMBINATION_PRODUCTIt was applied to the other group by aspiration.

the effect of oral care given by two different methods on the development of ventilator-associated pneumonia in patients connected to mechanical ventilators.

Sponsors

Ataturk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

• Patients on mechanical ventilator who have been in intensive care for at least 48 hours * Male and female patients over the age of 18 * Patients without thrombocytopenia, leukopenia and oral stomatitis, aphthae, candiasis, gingivitis * Patients whose respiratory support is provided by a mechanical ventilator * Patients who are considered to be able to provide mechanical ventilator support for 7 days * Patients without any respiratory-related infectious pathogens * Obtaining informed consent from the patient if he/she can give consent or from his/her guardian if he/she is unable to give consent. * It was determined as patients who did not undergo any intraoral surgical intervention.

Exclusion criteria

patients with pneumonia Patients younger than 18 years \-

Design outcomes

Primary

MeasureTime frameDescription
oral care application with standard oral care stick1 in 6 hoursAdministered with chlorhexidine gluconate solution.
Oral care application with a sucking oral care stick1 in 6 hoursAdministered with chlorhexidine gluconate solution.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026