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Recruiting NCT06354764

NCT06354764 Propensity to Hospitalize Patients From the ED in European Centers.

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Clinical Trial Summary
NCT ID NCT06354764
Status Recruiting
Phase
Sponsor Mario Negri Institute for Pharmacological Research
Condition Emergency Medicine
Study Type OBSERVATIONAL
Enrollment 162,000 participants
Start Date 2025-09-22
Primary Completion 2026-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
no intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 162,000 participants in total. It began in 2025-09-22 with a primary completion date of 2026-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

Inclusion Criteria: * Adult * Arrived at emergency department between 1 January 2021 and 31 December 2023 Exclusion Criteria: * None

Contact & Investigator

Central Contact

Chiara Pandolfini

✉ chiara.pandolfini@marionegri.it

📞 0039 02 39014 253

Principal Investigator

Guido Bertolini, MD

PRINCIPAL INVESTIGATOR

Istituto Di Ricerche Farmacologiche Mario Negri

Frequently Asked Questions

Who can join the NCT06354764 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Emergency Medicine. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06354764 currently recruiting?

Yes, NCT06354764 is actively recruiting participants. Contact the research team at chiara.pandolfini@marionegri.it for enrollment information.

Where is the NCT06354764 trial being conducted?

This trial is being conducted at Torino, Italy, Vercelli, Italy.

Who is sponsoring the NCT06354764 clinical trial?

NCT06354764 is sponsored by Mario Negri Institute for Pharmacological Research. The principal investigator is Guido Bertolini, MD at Istituto Di Ricerche Farmacologiche Mario Negri. The trial plans to enroll 162,000 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology