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Clinical Trials in France / NCT06494293
Starting soon Observational

How Many Patients Suffering Major Trauma Would be Eligible for a Pre-hospital Transfusion

NCT06494293 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-04
Last updated
2024-12-31

Condition(s) studied

Trauma Injury

Investigational drug(s) / intervention(s)

Data Collection

Data Collection: Collection of medical data from MICU intervention file and patient medical files from participating centres

Study summary

The aim of the study is to measure the number of patients being cared for by a medical team for major trauma who could benefit from a transfusion labile blood products and thus provide a scientific argument in favour of supplying labile blood products to pre-hospital

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria : * Patients over 18 * Taken care of by a MICU team from participating centres * Victims of major trauma requiring transport to an emergency/recovery unit or declared dead during care * Informed and did not object to the collection of his data for research purposes during his lifetime Exclusion Criteria : * Traumatological reason for departure not confirmed in the emergency medical services report * Patient care of by the MICU for secondary transport (transport from one hospital to another) * Patient died without resuscitation by a professional * Patient with manifest isolated closed head injury * Patient deprived of civil rights

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Resuscitation Services (SMUR) Ballanger - Centre Hospitalier Intercommunal Robert Ballanger Aulnay-sous-Bois France
Resuscitation Services (SAMU/SMUR) - Hôpital NOVO -Beaumont/Oise Site Beaumont-sur-Oise France
Resuscitation Services (SAMU/SMUR) - Hôpital NOVO -Pontoise Site Pontoise France
Resuscitation Services (SMUR) Delafontaine - Centre Hospitalier de Saint-Denis Saint-Denis France

More Hôpital NOVO trials in France

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 NCT06494293 on ClinicalTrials.gov ↗ ← All trials in France