External Validation of the FedHist Dynamic Early Warning Model for Mortality Risk in Critically Ill Patients: A Prospective Multicenter Study

ConditionICU
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSoutheast University, China

About this trial

The purpose of this study is to assess how accurately FedHist, an artificial intelligence model, predicts the risk of death in critically ill patients. Patients in intensive care units (ICUs) can become worse quickly. Updating risk estimates as new clinical information becomes available may help identify patients at higher risk. FedHist uses routinely collected clinical information to estimate a patient's risk of dying in the ICU within the next 24 hours. These estimates are updated every 6 hours.

This study will evaluate FedHist prospectively across several hospitals. The model will be integrated into hospital clinical information systems, and its predictions will be compared with observed patient outcomes. The study aims to determine whether FedHist provides accurate predictions across hospitals with different patient populations and clinical practices.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Admission to a participating ICU

Disqualifiers

Age younger than 18 years.

Expected ICU length of stay shorter than 24 hours.

Refusal to provide written informed consent.

Trial population

All patients admitted to the participating ICU

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Risk of mortality

    Other intervention

    Patients admitted to the ICU with different risk of mortality

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

ICU mortality

The proportion of patients who die from any cause during the ICU stay, with follow-up capped at 90 days after ICU admission. For patients whose ICU stay exceeds 90 days, vital status at day 90 will be used to determine the mortality outcome.

Time frame
From ICU admission to ICU discharge or 90 days after ICU admission, whichever occurs first.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: