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The effect of oral care program on pulmonary infection in intensive care unit

Effect of oral care program on prevention of ventilator-associated pneumonia in intensive care unit patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017101631200N2
Enrollment
80
Registered
2017-10-23
Start date
2016-11-21
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

ventilator-associated pneumonia. Other postprocedural respiratory disorders

Interventions

Intervention 1: Adjusting the pressure of the cuff of the endotracheal tube 20 using a special manometer.Brushing all internal and external surfaces of the teeth, gums and tongue for 2 min using a ba
Prevention
Adjusting the pressure of the cuff of the endotracheal tube 20 using a special manometer.Brushing all internal and external surfaces of the teeth, gums and tongue for 2 min using a baby toothbrush an

Sponsors

Isfahan University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Having intubation during study, Age between 18 to 65 years, Admision on ICU less than 12 hours, No further intubation, No extreme trauma of the face and mouth, No current hospitalization in other parts of the hospital, No pregnancy, Not having chronic disease and immune disorder, Patient with natural teeth, Lack of lung disease, Pneumonia and Sepsis according to CPIS tools. Exclusion Criteria: Transferring the patient from ICU or his/her death, Unwillingness to continue the study from the patient's legal guardian, Less than 48 hours under mechanical ventilation, Removing intubation before end of study, Allergic to chlorhexidine

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ventilator-Associated Pneumonia. Timepoint: First, Third, Fifth Day. Method of measurement: CPIS.

Secondary

MeasureTime frame
Oral Health. Timepoint: Daily for 5 days. Method of measurement: BOAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVajihe Atashi

Isfahan University of Medical Science

vajiheatashi@gmail.comvajiheatashi@yahoo.com+98 314390115

Outcome results

None listed

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