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the effects of oral rise with 0/2 and 2% chlorhexidine on oropharyngeal colonization and ventilator associated pneumonia

the effects of oral rise with 0/2 and 2% chlorhexidine on oropharyngeal colonization and ventilator associated pneumonia in adult intensive care units

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015100624382N1
Enrollment
112
Registered
2015-11-26
Start date
2015-04-05
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 acute lower respiratory infections

Interventions

Intervention 1: In control group, oral care protocol include, suction, oral assessment, brushing and rubbing saturated oral foam application of chlorhexidine 0/2% 10ml on gum, mucosa, teeth, hard pal
Prevention
Treatment - Drugs
In control group, oral care protocol include, suction, oral assessment, brushing and rubbing saturated oral foam application of chlorhexidine 0/2% 10ml on gum, mucosa, teeth, hard palate, every 12 ho
In intervention group, oral care protocol include, suction, oral assessment, brushing and rubbing saturated oral foam application of chlorhexidine 2% 10ml on gum, mucosa, teeth, hard palate, every 12

Sponsors

Vice chancellor for research of Shiraz University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18 years and older; informed consent; patients intubated and who on mechanical ventilation within 48 hours of admission; without a clinical diagnosis of pneumonia at the time of admission ; not to be pregnant ; without significant oral, facial trauma; not to readmitted to the ICU ; without known hypersensitivity to chlorhexidine; without an immunosuppression (disease or drug induced, e.g. organ transplant patient or those on long term steroid therapy); not to hospitalized for burn injury. Exclusion criteria: aspiration; a diagnosed thrombocytopenia (platelet less than 40000); INR above 2 or other coagulopathy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Oropharyngeal colonization. Timepoint: before intervention and if had exclusion criteria. Method of measurement: send culture and report semiquantitative.

Secondary

MeasureTime frame
Ventilator associated pneumonia. Timepoint: before, during and until 48hours and if had exclusion criteria. Method of measurement: clinical pulmonary infection score and clinical diagnose and start new antibiotic by intensivist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Zahed

Shiraz University of Medical Sciences-Fatemeh (PBUH) School of Nursing & Midwifery

lailazahed57 @ gmail. com;+98 71 3647 4257

Outcome results

None listed

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