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ThoRAciC Trauma IntubatiON Risk Score for Blunt Trauma

ThoRAciC Trauma IntubatiON Risk Score for Blunt Trauma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05637944
Acronym
TRACTIONS
Enrollment
1000
Registered
2022-12-06
Start date
2022-10-01
Completion date
2024-10-01
Last updated
2024-01-31

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

Conditions

Trauma Chest

Keywords

trauma; chest trauma

Brief summary

The primary objective of this study is the evaluation of risk factors associated with orotracheal intubation in blunt chest trauma patients not intubated on the field and not fulfilling the criteria for intubation based on the Glasgow Coma scale score with the building of a predictive score based on those findings taking into account the clinical, laboratory and radiologic tests performed within 6 hours from hospital admission.

Detailed description

Multicentre, prospective, observational study. All the consecutive blunt thoracic trauma patients consecutively admitted at the participating institutions' Emergency Department (ED) will be considered for enrolment. The primary outcome measure will be the need for orotracheal intubation for primary respiratory failure lasting at least 48 hours within 7 days after trauma. The secondary outcome measures related to analgesia are: the basal analgesia protocol received during the first 7 days from ED admission and the median cumulative dose of morphine-equivalents received as rescue therapy during the first 7 days after trauma. The secondary outcome measure related to the sonographic evolution of thoracic lesions is the global and regional LUS.

Interventions

PROCEDUREoro tracheal intubation

chest trauma requiring oro tracheal intubation

Sponsors

Azienda Ospedaliero-Universitaria Careggi
CollaboratorOTHER
Ospedale di Circolo e Fondazione Macchi, Varese
CollaboratorUNKNOWN
Trauma Center Pisa
CollaboratorUNKNOWN
Ospedale Santa Maria della Scaletta di Imola
CollaboratorUNKNOWN
Azienda Ospedaliera di Perugia
CollaboratorOTHER
Ospedale Policlinico San Martino
CollaboratorOTHER
Azienda Ospedaliero-Universitaria Maggiore della Carità di Novara
CollaboratorUNKNOWN
Ospedale S. Giuseppe (Empoli)
CollaboratorUNKNOWN
Pronto Soccorso Ospedale Misericordia Grosseto
CollaboratorUNKNOWN
Ospedale Bufalini - Cesena
CollaboratorUNKNOWN
Azienda Ospedaliero-Universitaria di Padova
CollaboratorUNKNOWN
ASST Papà Giovanni XXIII Bergamo
CollaboratorUNKNOWN
Pronto Soccorso e Medicina d'Urgenza Latisana
CollaboratorUNKNOWN
Humanitas Research Hospital IRCCS, Rozzano-Milan
CollaboratorOTHER
Azienda Usl di Bologna
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Blunt thoracic trauma with a documentable lesion (T-AIS ≥ 2) * Age ≥ 18 years * GCS \> 8 at ED admission * Total body CT scan available performed within 6 hours from ED admission

Exclusion criteria

* \- Penetrating thoracic trauma * Age \< 18 years * GCS \<= 8 at ED admission * Patients already intubated at ED arrival * Do not intubate order, for any reason * Intubation for Urgent/Emergent surgery within 24 hours from hospital arrival

Design outcomes

Primary

MeasureTime frame
needing for oro-tracheal intubation within day 7th from admission7 days

Countries

Italy

Contacts

Primary ContactLorenzo Gamberini, MD
lorenzo.gamberini@ausl.bologna.it0039 051 6478215

Outcome results

None listed

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