An Observational study to compare the clinical outcomes of Ventilator Associated Events among COVID-19 and non COVID ICU patients.
Not Applicable
- Conditions
- Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
- Registration Number
- CTRI/2021/08/035444
- Lead Sponsor
- ilavati hospital and research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients who are above 18 years old and are admitted to the ICU and require mechanical ventilation for more than 2 days
Exclusion Criteria
Patients on ECMO, ventilated for less than 48 hours, on NIV, who do not acheive stable ventilator settings after intubation or those who receives mechanical ventilation for more than 24 hours before ICU admission
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measured will be the rates of VAEs.Timepoint: 4 weeks
- Secondary Outcome Measures
Name Time Method The secondary outcomes include ICU mortality, duration of mechanical ventilation, successful extubation and tracheostomy. <br/ ><br>Timepoint: 4 weeks