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How Molecular Testing Improves Diagnosis and Treatment of Ventilator Associated Pneumonia from Gram Negative Bacteria in ICU Patients

Utility of molecular over traditional diagnostic method in diagnosis and management of ventilator associated pneumonia caused by Gram negative bacteria in intensive care unit - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/084715
Enrollment
184
Registered
2025-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: J189- Pneumonia, unspecified organism

Interventions

Control Intervention1: nil: nil

Sponsors

Dr Avinash Agrawal
Lead Sponsor
Dr Krishna Priya Agrawal
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: patients having clinically defined VAP according to CDC Age more than or equal to 18 years

Exclusion criteria

Exclusion criteria: Patients with evidence of chest infection prior to intubation or within 48 hours of mechanical ventilation Patients with severely immunocompromised state such as Acquired Immune Deficiency Syndrome organ transplant patients terminal stage of malignancy Patients whose sample could not be obtained Patients who are not willing to participate or give consent

Design outcomes

Primary

MeasureTime frame
To study the outcome 28 days mortality of early molecular identification of Gram negative organisms causing VAP and identification of common carbapenem resistant genes KPC IMP VIM NDM or OXA 48 compared with traditional culture methodsTimepoint: At baseline 4 weeks and 90 days

Secondary

MeasureTime frame
To compare the change in targeted antibiotic therapy selection according to molecular method and culture methodTimepoint: 2 days;To compare the change in Clinical Pulmonary Infection Score on third day of management on the basis of molecular method and culture methodTimepoint: 3 days;To compare the effect of diagnosis and management of VAP by both the methods on 90 days mortalityTimepoint: 90 days

Countries

India

Contacts

Public ContactProf Avinash Agrawal

King Georges Medical University Lucknow

avinashagrawal@kgmcindia.edu9838677999

Outcome results

None listed

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