The effects of oral care program on oropharyngeal complications and the Occurrence of ventilator associated pneumonia

Not Applicable

Recruiting

• Conditions: Condition 1: ventilator associated pneumonia. Condition 2: oropharyngeal complications.; Ventilator associated pneumonia; J95.851

• Registration Number: IRCT20191012045066N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Patient will have an endotracheal tube
Do not have mucosal inflammation or severe trauma to the mouth
Do not have Chronic Disease and Immune Deficiency
Have teeth
Do not have reentubation
Be the first day of patient intubation

Exclusion Criteria

Insertion a tracheostomy for the patient during the study
The obvious aspiration
Reduce platelet count to less than 40000
Increase INR to more than 2
Transfer or discharge the patient to another ward before the seventh day
Diagnose pneumonia within the first 48 hours after mechanical ventilation is started

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Clinical pneumonia infection score. Timepoint: Before the intervention, on the fourth and seventh days of the intervention. Method of measurement: Modified clinical pneumonia infection score.;Oral Health Score. Timepoint: On the second, fourth and seventh days of the intervention. Method of measurement: Beck Oral Assessment Scale.;Oral Health Score. Timepoint: On the second, fourth and seventh days of the intervention. Method of measurement: Mucosal Plaque Score.