Impact of Nanosil and Chlorhexidine on ventilator associated pneumonia
Not Applicable
- Conditions
- Ventilator Associated Pneumonia.Pneumonia organism unspecified
- Registration Number
- IRCT2017091636194N1
- Lead Sponsor
- Vice chancellor for research Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
aged between 18 and 70 years old; no clear maxillofacial trauma; having tracheal tube, locating the patient under the mechanical ventilator; no pneumonia or previous respiratory infections; utmost 48 hours have passed since the onset of intubation; no ban and having no alergia on using mouthwash;
Exclusion criteria: death before the end of intervention; extubation before the end of intervention; transfer the patient to other wards or hospital among the intervention; other diagnostic or therapeutic procedure on mouth and pharynx or trashea.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occurance of ventilator associated pneumonia. Timepoint: First day and fifth day. Method of measurement: Standard modified clinical pulmonary infection score.
- Secondary Outcome Measures
Name Time Method Degree of dysfunction of organs and prediction of mortality. Timepoint: First day and fifth day. Method of measurement: Standard sepsis related organ failure assessment tool.;Degree of consciousness. Timepoint: First day and fifth day. Method of measurement: Standard glascow coma scale.