Skip to content

In-Hospital Electronic Registry of Severe Trauma of the Fondazione I.R.C.C.S. Policlinico San Matteo

In-Hospital Electronic Registry of Severe Trauma of the Fondazione I.R.C.C.S. Policlinico San Matteo (TRAUMA REGISTRY S. MATTEO)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06930820
Acronym
STRAP register
Enrollment
4000
Registered
2025-04-16
Start date
2022-07-01
Completion date
2032-07-07
Last updated
2025-04-16

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

Conditions

Patients Who Are Victims of Major Trauma

Brief summary

The objective of establishing an in-hospital Trauma Registry, aimed at collecting data on patients who are victims of major trauma and treated at our Center, is to develop a comprehensive and in-depth tool for the analysis and monitoring of clinical activity within a Level I Trauma Center. The purpose of building such databases-specifically the proposed Trauma Registry-is to provide the hospital with a unique instrument for analyzing and monitoring the epidemiology and management of a specific patient population. In light of recent developments in the hospital's newly implemented clinical care pathway (PDTA) for the management of polytrauma patients, and the strategic enhancement offered by the opening of a dedicated helipad for the reception of such patients, our working group is committed to promoting a tool that may, both in the short and long term, foster clinical and scientific advancement at the Fondazione I.R.C.C.S. Policlinico San Matteo in Pavia. Our general objective is the prospective collection of data on major trauma patients admitted to and treated at the Fondazione I.R.C.C.S. Policlinico San Matteo. Our primary objective is to evaluate in-hospital mortality, used as a qualitative indicator of the Trauma Center's performance, among patients with severe trauma managed at our institution.

Interventions

None listed

Sponsors

Fondazione IRCCS Policlinico San Matteo di Pavia
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

All consecutive patients presenting to the Emergency Department of the Fondazione I.R.C.C.S. Policlinico San Matteo who meet at least one of the following criteria will be included in the registry: * They were transported to the Emergency Department by Emergency Medical Services (AREU - Regional Emergency and Urgency Agency) with a diagnosis of Severe Trauma / Major Trauma or \- They arrived at the Emergency Department and were admitted with a diagnosis of trauma, and were found, upon completion of the secondary assessment, to have an Injury Severity Score (ISS) \>15

Exclusion criteria

There are no

Design outcomes

Primary

MeasureTime frameDescription
In-hospital mortality ratethrough study completion, an average of 10 yearsThe primary objective of the registry is to evaluate in-hospital mortality for patients with severe trauma treated at the Fondazione I.R.C.C.S. Policlinico San Matteo.

Secondary

MeasureTime frameDescription
Relationship between the severity of traumatic injuries, quantified using the Injury Severity Score (ISS), and in-hospital mortalitythrough study completion, an average of 10 yearsEvaluation of the relationship between the severity of traumatic injuries, quantified using the Injury Severity Score (ISS), and in-hospital mortality.
Hospital length of stay and its relationship with the ISSthrough study completion, an average of 10 yearsEvaluation of hospital length of stay and its relationship with the ISS.
Intensive Care Unit (ICU) length of stay and its relationship with the ISSthrough study completion, an average of 10 yearsEvaluation of Intensive Care Unit (ICU) length of stay and its relationship with the ISS.

Countries

Italy

Contacts

Primary ContactLuca Ansaloni, MD
l.ansaloni@smatteo.pv.it+39 0382 502490

Outcome results

None listed

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