Actively Recruiting

Age: 0 - 24Weeks
All Genders
NCT07109791

National Surveillance and Prevention of Neonatal VAP

Led by University of Alberta · Updated on 2026-02-09

1500

Participants Needed

1

Research Sites

178 weeks

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

U

University of Calgary

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to improve how hospital-acquired lung infections (called ventilator-associated pneumonia, or VAP) are diagnosed, treated and prevented in very low birth weight (VLBW) infants, babies born very early (preterm) or very small who often require respiratory support in hospital's neonatal intensive care units (NICUs). The main questions it aims to answer are: * How often do very-low-birth-weight (VLBW) infants get ventilator-associated pneumonia (VAP) in hospitals across Canada? * How often are these VAP infections caused by germs that are resistant to antimicrobials (also known as antimicrobial-resistant organisms or AROs)? * What types of antimicrobial-resistant germs (AROs) are causing them? * How are these infections being treated with antibiotics, and can we reduce unnecessary antibiotic use? * Which diagnostic definition is the best and most accurate for diagnosing VAP in newborns, based on real patient data and expert agreement? * Can we use this information to create clear, evidence-based guidelines that help hospitals prevent and treat VAP in the same, effective way? Researchers will compare how different hospitals define, report, and manage VAP to devise a shared, evidence-based approach that will lead to more accurate diagnoses and better treatment and outcomes for neonatal VAP. Researchers will: * Use data already collected in hospital records (per existing standard of clinical care). * Analyse how often VAP occurs, how it is diagnosed, and how it is treated * Work with experts and hospitals to develop and implement a standard, evidence-based plan for diagnosing, managing and preventing VAP in newborns The overarching goal is to create a clear, nationwide approach to ensure hospitals across Canada care for preterm babies in a standardized manner, reduce infection rates, avoid unnecessary antibiotic use, and improve outcomes for these vulnerable infants.

CONDITIONS

Official Title

National Surveillance and Prevention of Neonatal VAP

Who Can Participate

Age: 0 - 24Weeks
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All VLBW infants admitted to participating tertiary NICUs in Canada
  • All neonatal VAP events diagnosed based on the physicians' discretion
Not Eligible

You will not qualify if you...

  • Infants with major congenital anomalies
  • Infants with moribund status on admission

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Royal Alexandra Hospital

Edmonton, Alberta, Canada, T5H 3V9

Actively Recruiting

Loading map...

Research Team

D

Dr. Joseph Ting, Staff Neonatologist and Clinical Research Professor

CONTACT

C

Christie (Zixuan) Li, Clinical Research Coordinator, BSc, MSc

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here