FindTrial
Sign In

An Observational study to compare the clinical outcomes of Ventilator Associated Events among COVID-19 and non COVID ICU patients.

A Prospective comparative study on the clinical outcomes of Ventilator Associated Events among COVID-19 and non COVID ICU patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/08/035444
Enrollment
84
Registered
2021-08-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere

Interventions

Control Intervention1: NIL: NIL

Sponsors

Lilavati hospital and research centre
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
The primary outcome measured will be the rates of VAEs.Timepoint: 4 weeks—

Secondary

MeasureTime frame
The secondary outcomes include ICU mortality, duration of mechanical ventilation, successful extubation and tracheostomy. Timepoint: 4 weeks—

Countries

India

Contacts

Public ContactDr Susan Philip

Lilavati Hospital and Research Centre

conradruivas@lilavatihospital.com9820125932

Outcome results

None listed

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