Actively Recruiting
Asia Pediatric Intensive Care Epidemiology and Outcomes Study
Led by KK Women's and Children's Hospital · Updated on 2026-04-08
10000
Participants Needed
2
Research Sites
39 weeks
Total Duration
On this page
Sponsors
K
KK Women's and Children's Hospital
Lead Sponsor
K
King Chulalongkorn Memorial Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to improve care for critically ill children admitted to pediatric intensive care units ICUs across Asia. It will describe the health profiles and outcomes of these patients, identify risk factors linked to poorer results, and develop quality measures to compare ICU performance. The study will also create and train artificial intelligence models to predict mortality, length of ICU stay, and use of resources in this diverse pediatric population. The study will collect detailed data on patient demographics, clinical features, ICU treatments, quality indicators, and outcomes from multiple hospitals. It will follow a prospective observational design, recruiting all pediatric ICU admissions with allowance for random sampling in resource-limited sites. A subgroup analysis will focus on children with chronic complex conditions, who represent a significant portion of ICU admissions and resource use. Participants will be monitored throughout their ICU stay, with data collected on outcomes such as mortality at 28 and 60 days, ventilator use duration, ICU length of stay, infections, accidental extubations, thrombosis, and unplanned ICU readmissions. The study will analyze this information to enhance understanding of pediatric critical illness and guide improvements in ICU care. Recruitment will last one year per site, starting at different times depending on ethics approvals.
CONDITIONS
Brief Title
Asia Pediatric Intensive Care Epidemiology and Outcomes Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients admitted to the pediatric ICUs of participant hospitals
You will not qualify if you...
- No consent
Research Team
J
Judith Ju Ming Wong, MBBCh BAO
C
Cecilia Chandran
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