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Evaluation of Parameters Collected From Routine Data for the Diagnosis of Sepsis and Septic Shock and Their Influence on Time to Diagnosis and Patient Outcome

Evaluation of Parameters Collected From Routine Data for the Diagnosis of Sepsis and Septic Shock and Their Influence on Time to Diagnosis and Patient Outcome (QUICK-SEPSIS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05383963
Enrollment
10000
Registered
2022-05-20
Start date
2022-07-15
Completion date
2027-12-31
Last updated
2025-12-01

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

Conditions

Sepsis, Septic Shock

Brief summary

Retrospective observational study to develop a Machine Learning Algorithm to evaluate parameters collected from routine data for the diagnosis of sepsis and septic shock and their influence on time to diagnosis and patient outcome.

Detailed description

Retrospective routine data from the medical records of the department of anesthesiology and operative intensive care from 01. 01. 2007 to 31. 12. 2021 are analyzed in digital form. The first step is the development of a machine learning algorithm (MLA). This MLA will be validated and analyzed for his predictive value with regard to early diagnosis of sepsis/septic shock depending on the conceptual value of detection variables (Sepsis-3 vs. SIRS). Further analysis will focus on improvement of accuracy for the MLA and the effect of these detection variables on quality of treatment processes and also on economic consequences like cost and revenue. Timeline: 1. Conception and development of the ML Algorithm (6 months) 2. Identification and diagnostic validation of sepsis patients (6 months) 3. Secondary analyses (36 months)

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* age \>= 18 years * ICU stay of \> 24 hours

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Sepsis/septic shock01.01.2007 -31.12.2021Development of a machine learning algorithm (MLA) for the prediction of sepsis/septic shock from hospital routine data.

Secondary

MeasureTime frameDescription
Predictive accuracy01.01.2007 -31.12.2021Evaluation of the predictive accuracy (= predictive value) of the respective sepsis diagnostic algorithm (i.e. comparison of the concepts SIRS and Sepsis-3)
Diagnostic accuracy01.01.2007 -31.12.2021Identification of additional variables for diagnostic accuracy (laboratory values, clinical parameters and vital-sign monitor parameters and other relevant health data
Performance indicators01.01.2007 -31.12.2021Evaluation of performance indicators of clinical routine processes (Intensive care quality indicators)
Case costs01.01.2007 -31.12.2021Case costs related to hospitalization
Revenues01.01.2007 -31.12.2021Revenues related to hospitalization

Countries

Germany

Contacts

Primary ContactClaudia Spies, MD, Prof.
claudia.spies@charite.de+49 30 450 55 11 02

Outcome results

None listed

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