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Predictive and Advanced Analytics in Emergency Medicine - Neurological Deficits

Predictive and Advanced Analytics in Emergency Medicine - Neurological Deficits

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06245694
Acronym
PAN-EM-NEURO
Enrollment
50000
Registered
2024-02-07
Start date
2022-01-01
Completion date
2030-01-01
Last updated
2024-11-22

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

Conditions

Artificial Intelligence, Neurologic Manifestations, Resource Allocation

Brief summary

Future predictive modeling in emergency medicine will likely combine the use of a wide range of data points such as continuous documentation, monitoring using wearables, imaging, biomarkers, and real-time administrative data from all health care providers involved. Subsequent extensive data sets could feed advanced deep learning and neural network algorithms to accurately predict the risk of specific health conditions. Moreover, predictive analytics steers towards the development of clinical pathways that are adaptive and continuously updated, and in which healthcare decision-making is supported by sophisticated algorithms to provide the best course of action effectively and safely. The potential for predictive analytics to revolutionize many aspects of healthcare seems clear in the horizon. Information on the use in emergency medicine is scarce. Aim of the study is to evaluate the performance of using routine-data to predict resource usage in emergency medicine using the commonly encountered symptom of acute neurologic deficit. As an outlook, this might serve as a prototype for other, similar projects using routine medical data for predictive analytics in emergency medicine.

Interventions

None listed

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

* Female and Male subjects * Age ≥ 18 years

Exclusion criteria

\- none

Design outcomes

Primary

MeasureTime frameDescription
Prediction model1.1.2025to be developed

Countries

Austria

Contacts

Primary ContactJan Niederdöckl, MD
jan.niederdoeckl@meduniwien.ac.at0042 40 400 19640

Outcome results

None listed

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