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A study to evaluate the performance of software ‘AITRICS-VC’ for predicting sepsis, and major adverse events in a general ward inpatient using EMR data

Prospective, Non-interventional, Descriptive, Single-center study after approval to evaluate the performance of software ‘AITRICS-VC’ for predicting sepsis, and major adverse events in a general ward inpatient using EMR data

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008466
Enrollment
10500
Registered
2023-05-25
Start date
2023-06-05
Completion date
Unknown
Last updated
2024-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Aitrics
Lead Sponsor
Keimyung University Dongsan Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: To be eligible for this clinical trial, participants must meet all of the following criteria: 1. Adult men and women aged 19 years or older 2. Patients admitted to six general wards of four selected departments within Keimyung University Dongsan Hospital within 8 months after IRB approval 3. Patients for whom age, systolic blood pressure, diastolic blood pressure, heart rate, respiratory rate, and body temperature information can be obtained from the electronic medical record during hospitalization.

Exclusion criteria

Exclusion criteria: If any of the following exclusion criteria apply, the participant cannot be enrolled in this clinical trial: 1. Patients who have already been diagnosed with sepsis and are receiving treatment 2. Participants deemed inappropriate for the study by the investigator due to factors that may affect the validity of the evaluation or other reasons.

Design outcomes

Primary

MeasureTime frame
AUROC of the Sepsis Prediction Algorithm(SEPS) for Early Detection of Sepsis within 4 Hours;AUROC of the Major Adverse Events Prediction Algorithm(MAES) for Early Detection of Major Adverse Events within 6 Hours

Secondary

MeasureTime frame
Sensitivity as evaluated by the SEPS algorithm for the prediction of sepsis;Specificity as evaluated by the SEPS algorithm for the prediction of sepsis;Comparison of the AUROC for the SEPS algorithm and qSOFA, SOFA score for predicting sepsis;Comparison of the sepsis detection time between the SEPS Algorithm and qSOFA, SOFA score for sepsis prediction;Sensitivity as evaluated by the MAES algorithm for the prediction of major adverse events;Specificity as evaluated by the MAES algorithm for the prediction of major adverse events;Comparison of the AUROC for the MAES algorithm and MEWS,NEWS score for predicting major adverse events;Comparison of the major adverse events detection time between the MAES Algorithm and MEWS, NEWS score for major adverse events prediction

Countries

Korea, Republic of

Contacts

Public ContactGyeong Im Yu

Keimyung University Dongsan Hospital

rki0411@hanamil.net+82-53-258-7217

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026