ThoRAciC Trauma IntubatiON Risk Score for Blunt Trauma

NCT05637944 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2024-01-31

No results posted yet for this study

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.

Conditions

  • Trauma Chest

Interventions

PROCEDURE

oro tracheal intubation

chest trauma requiring oro tracheal intubation

Sponsors & Collaborators

  • Azienda Ospedaliero-Universitaria Careggi

    collaborator OTHER
  • Ospedale di Circolo e Fondazione Macchi, Varese

    collaborator UNKNOWN
  • Trauma Center Pisa

    collaborator UNKNOWN
  • Ospedale Santa Maria della Scaletta di Imola

    collaborator UNKNOWN
  • Azienda Ospedaliera di Perugia

    collaborator OTHER
  • Ospedale Policlinico San Martino

    collaborator OTHER
  • Azienda Ospedaliero-Universitaria Maggiore della Carità di Novara

    collaborator UNKNOWN
  • Ospedale S. Giuseppe (Empoli)

    collaborator UNKNOWN
  • Pronto Soccorso Ospedale Misericordia Grosseto

    collaborator UNKNOWN
  • Ospedale Bufalini - Cesena

    collaborator UNKNOWN
  • Azienda Ospedaliero-Universitaria di Padova

    collaborator UNKNOWN
  • ASST Papà Giovanni XXIII Bergamo

    collaborator UNKNOWN
  • Pronto Soccorso e Medicina d'Urgenza Latisana

    collaborator UNKNOWN
  • IRCCS Humanitas - Rozzano (MI)

    collaborator UNKNOWN
  • Azienda Usl di Bologna

    lead OTHER_GOV

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-10-01
Primary Completion
2024-10-01
Completion
2024-10-01

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05637944 on ClinicalTrials.gov