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Clinical Trials in Italy / NCT06354764
Recruiting Observational

Propensity to Hospitalize Patients From the ED in European Centers.

NCT06354764 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2025-09-22
Last updated
2026-05-20

Condition(s) studied

Emergency Medicine

Investigational drug(s) / intervention(s)

no intervention

no intervention: no intervention

Study summary

The peer-to-peer comparison means center-to-center comparison, which requires adjusting for possible differences among centers to be fair and convincing. The first step to reach this goal is to develop a predictive model that accurately estimates each patient's probability of being admitted, starting from clinical conditions and boundary variables. Such a model would make it possible to calculate, for each ED, the expected hospitalization rate; that is, the hospitalization rate that would have been observed if the ED had behaved like the average of the EDs that provided the data to build the model itself. Comparing the observed hospitalization rate in the single ED with the expected rate derived from the model provides a rigorous method of comparing the department with the average performance, taking into account the characteristics of the patients treated and the conditions under which the ED operated. In other words, the predictive model represents the benchmark against which each ED is evaluated.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult * Arrived at emergency department between 1 January 2021 and 31 December 2023 Exclusion Criteria: * None

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Ospedale San Giovanni Bosco Torino Italy Recruiting
Ospedale Sant'Andrea Vercelli Italy Recruiting

More Mario Negri Institute for Pharmacological Research trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06354764 on ClinicalTrials.gov ↗ ← All trials in Italy