Clinical trial Recruiting at 2 sites Observational Ages 5 to 16

Smart Discharges for Older Children after Sepsis

Official title: Smart Discharges for Older Children: A Cohort Study to Develop Prognostic Algorithms for Post-discharge Readmission and Mortality Among Children Over 5 Years of Age

Run by University of British Columbia · NCT07629154 · Data updated 2026-11-12

This observational study follows children aged 5 to 16 who were treated for sepsis to see if a risk score built from their hospital stay can predict who might die or have poor health after going home.

Quick facts

Study typeObservational
Ages5 Years to 16 Years
SexAll
Enrollment4000 (estimated)
SponsorUniversity of British Columbia
Academic / other
Locations7 sites (San Francisco, California and 6 other locations)
StatusRecruiting
StartedJanuary 2, 2024
Main results expectedApril 2027
Study endsApril 2027
Registry record updatedJune 15, 2026
Trial IDNCT07629154 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 5 to 16 years admitted with proven or suspected sepsis and whose guardians consent and provide contact information for follow-up.

Probably not a fit

Children without elevated post-discharge risk or those outside the catchment area or follow-up capabilities may see no direct benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multinational, observational cohort study collects clinical and social data from children admitted with suspected or proven sepsis to develop and validate a risk-prediction model for post-discharge mortality in the 6 months after discharge. It also assesses health-related quality of life and functional status up to a year post-discharge. The study enrolls participants at admission and follows them for six months, aiming to create a scalable post-discharge support approach within resource-limited settings. No active intervention is given; the focus is on model development and outcome tracking to inform post-discharge care decisions. The work builds on prior Smart Discharges efforts and involves multiple institutions across high-income and low- to middle-income countries.

Why it matters

Potential benefit: If successful, the model could help clinicians and families identify high-risk children after discharge and tailor follow-up and resources to reduce mortality and improve quality of life.

How similar studies have gone: Previous Smart Discharges work has shown promise in predicting post-discharge risk in pediatric populations, supporting the potential for scale-up in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • The Rwanda Paediatric Association
    Kigali, Rwanda
    Recruiting
  • Catholic University Of Health And Allied Sciences
    Mwanza, Tanzania
    Recruiting
  • University of California, San Francisco
    San Francisco, California, United States
    Not yet recruiting
  • Weill Cornell Medicine
    Ithaca, New York, United States
    Not yet recruiting
  • University of Washington
    Seattle, Washington, United States
    Not yet recruiting
  • BC Children's Hospital Research Institute
    Vancouver, British Columbia, Canada
    Active not recruiting
Show 1 more location
  • Walimu
    Mbarara, Uganda
    Completed

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.