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Comparing an Automated to a Conventional Sepsis Clinical Prediction Rule

Comparing an Automated to a Conventional Sepsis Clinical Prediction Rule

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01505478
Enrollment
0
Registered
2012-01-06
Start date
2012-07-31
Completion date
Unknown
Last updated
2017-04-05

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

Conditions

Sepsis

Keywords

Sepsis, Clinical Prediction Rule, Clinical Informatics, Machine Learning

Brief summary

The investigators will conduct a prospective cohort study to compare an automated sepsis severity score to a conventional clinical prediction rule to risk stratify patients admitted from the emergency department (ED) with suspected infection for 28 day in-hospital mortality.

Interventions

None listed

Sponsors

New York University
CollaboratorOTHER
United States Department of Defense
CollaboratorFED
Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All consecutive adult (age 18 or older) Emergency Department (ED) patients during the study period that have been admitted from the ED and identified by the treating clinician to have a suspected infection at the time of ED disposition will comprise our study population.

Exclusion criteria

* No patients will be excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
28 day in-hospital mortalityThe primary endpoint is the AUC of a model to predict 28 day all cause in-hospital mortality. Patients discharged or transferred to another hospital before 28 days will be assumed to be alive at 28 days.

Secondary

MeasureTime frameDescription
ICU AdmissionThe secondary endpoint is ICU admission from the ED or within 24 hours from the floor.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026