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Clinical Trials in Canada / NCT07629154
Recruiting Observational

Smart Discharges for Older Children

NCT07629154 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2024-01-02
Last updated
2026-06-15

Condition(s) studied

Sepsis

Investigational drug(s) / intervention(s)

No Intervention: Observational Cohort

No Intervention: Observational Cohort: This is a non-interventional study

Study summary

This study is an observational multi-country cohort study that aims to build algorithms that can identify children between 5 and 16 years of age admitted for proven or suspected sepsis who are at risk of mortality after they are discharged in East Africa.

In low- and middle-income countries, about 5% of children discharged after hospitalization for sepsis will die in the weeks after returning home. Doctors and parents are often unaware of this period of vulnerability and are poorly equipped to identify or handle this critical situation. This project builds on past work that developed and evaluated models and the Smart Discharges program to predict, during hospitalization, an individual child's risk of recurrent illness and mortality, as well as to provide additional post-discharge support to at-risk children.

Participants will be enrolled from facilities once they are admitted, collecting clinical and social variables. They will then be followed until 6 months post-discharge to understand what happens to them after they return home. This data will be evaluated to identify which variables collected at facilities can be predictive of mortality and recurrent illness after discharge.

Eligibility

Sex
ALL
Min age
5 Years
Max age
16 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 0 and 16 years admitted to pediatric ward of hospital for proven or suspected infection * Provide informed consent * Ability to provide contact information (phone number or address) for phone or in-person follow-up Exclusion Criteria: * Child lives outside of the catchment area of a study site * Admitted for elective procedures, trauma, or short-term observation * Language barriers

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
University of California, San Francisco San Francisco California Not Yet Recruiting
Weill Cornell Medicine Ithaca New York Not Yet Recruiting
University of Washington Seattle Washington Not Yet Recruiting
BC Children's Hospital Research Institute Vancouver British Columbia Active Not Recruiting
The Rwanda Paediatric Association Kigali Rwanda Recruiting
Catholic University Of Health And Allied Sciences Mwanza Tanzania Recruiting
WALIMU Mbarara Uganda Completed

More University of British Columbia trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07629154 on ClinicalTrials.gov ↗ ← All trials in Canada