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Effect of thymus essential oil in prevention of ventilator associated pneumonia

Phase 3
Recruiting
Conditions
Ventilator associated pneumonia.
Pneumonia in other diseases classified elsewhere
Registration Number
IRCT20170220032672N2
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
106
Inclusion Criteria

Aged 18 years and above
Under invasive mechanical ventilation

Exclusion Criteria

Clinical Pulmonary Infection Score (CPIS) more than 6
history of allergy
sepsis
acute phase Cancer
trauma to the jaw, face and chest

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Percentage of patients with ventilator associated pneumonia. Timepoint: CPIS measurements at the beginning of the study (before the intervention) and 5th and 10th days after the began of intervention. Method of measurement: Clinical Pulmonary Infection Score (CPIS).
Secondary Outcome Measures
NameTimeMethod
Peak inspiratory pressure and plateau pressure. Timepoint: at the beginning of the study (before the intervention) and 5th and 10th days after the began of intervention. Method of measurement: monitoring of ventilator data.;SpO2, SaO2. Timepoint: at the beginning of the study (before the intervention) and 5th and 10th days after the began of intervention. Method of measurement: pulse oxymeter and arterial blood gas.;Rapid Shallow Breathing Index (RSBI). Timepoint: at the beginning of the study (before the intervention) and 5th and 10th days after the began of intervention. Method of measurement: monitoring of ventilator data.
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