NCT06259812

Brief Summary

A large number of different organ functions are recorded in real time for patients being monitored in an intensive care unit. On the one hand, the measured values collected are used for continuous monitoring of vital parameters, e.g. blood pressure, heart rate and respiratory rate, but are also evaluated several times a day in conjunction with other data as part of ward rounds. In both cases, continuous monitoring from a limited number of parameters, but also in the distinct evaluation with a more extensive set of analyzable parameters, there are limitations in the evaluability even with all the care and expertise available: In continuous analysis, interpretation is limited by the restricted number of continuously recorded parameters described above. Although a large number of such measurements are possible, and at least theoretically a larger number of parameters could be measured, patient-specific limits such as patient cooperation, medical limits such as the significance of the measured values in specific situations, but also economic limits are often decisive in this context. Although accurate conclusions can be drawn from the continuous and therefore complete representation of aspects of human physiology, the limitation of the available parameters reduces the interpretability of the synthesis of different statuses. In the broader, more comprehensive assessments during visits at specific points in time, on the other hand, there are limitations due to, among other things, point recordings of individual measured values and the predefined visit times. Even if limit values are (or can be) defined for the measured data, and a consequence, e.g. a therapy step, is initiated if these values are exceeded or not reached, this alert can only be initiated retrospectively if these values are exceeded and a consequence can only be initiated retrospectively. In this situation, a pathophysiological change is already so far advanced that in many cases a compensation mechanism no longer functions adequately and turns into a decompensation situation. In this situation, the patients affected in an intensive care unit are in many cases in mortal danger. Both situations, continuous recording of a limited number of parameters and the evaluation of extensive data in the form of a snapshot could be optimized despite the limitations mentioned. Without changing the collection of data (time, scope, etc.), the possibilities for optimizing their interpretation and the consequences that can be derived from the interpretation remain. The interpretation of the data is primarily determined by the interpreters as the method of interpretation. Current approaches attempt to use machine learning (ML) methods to predict individual situations that recognize adverse events in the given data and at the same time allow alarms to be triggered pre-emptively, i.e. before a life-threatening situation occurs. Furthermore, there are already studies on the change of early warning scores in time series, which are, however, limited in their informative value for longer prediction periods.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
8,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2024

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 7, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 14, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

May 1, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2024

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2025

Completed
Last Updated

October 15, 2024

Status Verified

October 1, 2024

Enrollment Period

5 months

First QC Date

February 7, 2024

Last Update Submit

October 12, 2024

Conditions

Outcome Measures

Primary Outcomes (4)

  • AUC-ROC for Prediction of Parameters of Early Warning Scores

    AUC-ROC for Prediction of Parameters of Early Warning Scores

    2010-01-01 to 2023-12-31

  • AUC-PRC for Prediction of Parameters of Early Warning Scores

    AUC-PRC for Prediction of Parameters of Early Warning Scores

    2010-01-01 to 2023-12-31

  • F1-Score for Prediction of Parameters of Early Warning Scores

    F1-Score for Prediction of Parameters of Early Warning Scores

    2010-01-01 to 2023-12-31

  • Confusion Matrix for Prediction of Parameters of Early Warning Scores

    Confusion Matrix for Prediction of Parameters of Early Warning Scores

    2010-01-01 to 2023-12-31

Secondary Outcomes (2)

  • SHAP Values for Prediction Models

    2010-01-01 to 2023-12-31

  • Confusion Matrix for Prediction of In Hospital-Mortality

    2010-01-01 to 2023-12-31

Interventions

Parameters of Early Warning Scores

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients treated in intensive care.

You may qualify if:

  • Treated in intensive care between 2010-01-01 and 2023-12-31 at the study center.

You may not qualify if:

  • None.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kepler University Hospital

Linz, Upper Austria, 4020, Austria

Location

Study Officials

  • Jens Meier, MD

    Johannes Kepler University

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 7, 2024

First Posted

February 14, 2024

Study Start

May 1, 2024

Primary Completion

September 15, 2024

Study Completion

September 15, 2025

Last Updated

October 15, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will not share

Locations