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Clinical application research of sepsis early warning system

Clinical application research of sepsis early warning system

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086816
Enrollment
Unknown
Registered
2024-07-11
Start date
2022-12-01
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

sepsis

Interventions

Gold Standard:The reference standard "The third international consensus definitions for sepsis and septic shock (sepsis-3)," published in the "Journal of the American Medical Association (JAMA, 2016).
Index test:Sepsis Early Warning Model Based on Next-Generation Artificial Intelligence Technology

Sponsors

Guangxi Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 91 Years

Inclusion criteria

Inclusion criteria: The criteria for sepsis patients included in the publicly available dataset mimic iv during the study period are as follows: 1) Diagnosis of sepsis according to Sepsis 3.0 criteria: ? Treatment with antibiotics ? Collection of biological fluids for microbial culture ? Evidence of accompanying organ dysfunction (i.e. SOFA score = 2); 2) Age greater than or equal to 18 years old. The criteria for recruiting doctors during the research period are as follows: 1) Having clinical diagnostic qualifications; 2) Voluntarily sign an informed consent form and participate in the study.

Exclusion criteria

Exclusion criteria: The exclusion criteria for sepsis patients in the publicly available dataset mimic iv during the study period are as follows: 1) Age<18 years old when admitted to the intensive care unit 2) No recorded deaths 3) Stop treatment (patients who die within 24 hours after the end of the data collection period, receive vasoconstrictive drugs at any time, and stop taking vasoconstrictive drugs at the end of the data collection period) 4) Unrecorded venous fluid intake The exclusion criteria for doctors during the study period are as follows: 1) External training and internship workers; 2) Medical workers who were not on duty during the investigation period.

Design outcomes

Primary

MeasureTime frame
Diagnostic Accuracy;

Secondary

MeasureTime frame
Antibiotic Usage Accuracy;Diagnostic Time;

Countries

China

Contacts

Public ContactYunyouHuang

Guangxi Normal University

hungyy4@gmail.com+86 188 1002 9186

Outcome results

None listed

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