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Diagnostic Accuracy in Sepsis

Diagnostic Accuracy of Clinical and Paraclinical Tools in Sepsis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03956043
Enrollment
1989
Registered
2019-05-20
Start date
2017-05-15
Completion date
2024-12-15
Last updated
2025-03-21

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

Conditions

Sepsis Syndrome

Brief summary

The sepsis syndrome has recently been more stringently defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection. Clinical and paraclinical tools are investigated for their ability to adequately recognize sepsis early.

Interventions

None listed

Sponsors

Oslo University Hospital
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

* Patients \>18 years old with suspected sepsis in the Emergency Department of Oslo University Hospital Oslo

Exclusion criteria

* Non

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracy in sepsiswithin 90 days after inclusionSensitivity, specificity, predictive values, AUC of clinical criteria of sepsis in the Emergency department, compared to post hoc assesment
Prognostic accuracy in sepsis90 days after inclusionSensitivity, specificity, predictive values, AUC of clinical criteria of sepsis in the Emergency department, compared to in hospital, 30 and 90 days mortality

Countries

Norway

Outcome results

None listed

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