Viewing Study NCT04760977



Ignite Creation Date: 2024-05-06 @ 3:48 PM
Last Modification Date: 2024-10-26 @ 1:57 PM
Study NCT ID: NCT04760977
Status: RECRUITING
Last Update Posted: 2022-08-29
First Post: 2021-02-16

Brief Title: Prehospital Management of Hypotensive Trauma in HEMS
Sponsor: Azienda Usl di Bologna
Organization: Azienda Usl di Bologna

Study Overview

Official Title: Prehospital Management of Hypotensive Trauma in HEMS
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SPITFIRE
Brief Summary: Up to today inadequate evidences and knowledge exist about the best prehospital management of hypotensive trauma patients and its clinical consequence on the in-hospital recovery and mortality

Also new emerging therapies such as prehospital blood transfusion and REBOA resuscitative endovascular balloon occlusion of the aorta are lacking strong evidences in eventually reducing hospital mortality and improving outcomes

Moreover prehospital emergency medicine is throughout Italy an heterogeneous system that has no unique standard operating procedures and even among HEMS helicopter emergency medical service management and therapies on complex trauma patients may vary upon local policies

With this study we aim to enroll hypotensive trauma patients and study factors of prehospital rescue that can be associated with in-hospital mortality and recovery eventually even with hospital outcome For each patients data as demographic kind of trauma mechanism injury scores therapies and maneuvers will be recorded and then analyzed in comparison with in-hospital data such as need for transfusion ABG parameters length of stay in-ward and ICU need of therapies like invasive ventilation and renal replacement therapy recovery and outcome
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None