Oral Care to Prevent Ventilator-associated Pneumonia

Ventilators, Mechanical Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05161962
• Other study ID #: AtaturkU-001
• Status: Completed
• Phase: N/A
• Start date: September 1, 2019
• Est. completion date: February 5, 2020

Study information

• Verified date: December 2021
• Source: Ataturk University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 57
• Est. completion date: February 5, 2020
• Est. primary completion date: January 23, 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 90 Years

Eligibility

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 -

Related Conditions & MeSH terms

• Pneumonia
• Ventilators, Mechanical

Intervention

Combination Product:
• One 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.
• It 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.

Locations

Country	Name	City	State
Turkey	Atatürk University	Erzurum

Sponsors (1)

Lead Sponsor	Collaborator
Ataturk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	oral care application with standard oral care stick	Administered with chlorhexidine gluconate solution.	1 in 6 hours
Primary	Oral care application with a sucking oral care stick	Administered with chlorhexidine gluconate solution.	1 in 6 hours