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Evaluation of Trauma Team Activation Criteria

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ClinicalTrials.gov Identifier: NCT01771861
Recruitment Status : Completed
First Posted : January 18, 2013
Last Update Posted : October 28, 2016
Sponsor:
Information provided by (Responsible Party):
University Hospital of North Norway

Brief Summary:

The aim of the study is to establish the predictive properties of our trauma team activation protocol, and its individual criteria, and if possible to suggest changes that reduce over- and undertriage.

The study will also give an overview of the frequency and type of emergency procedures at a university hospital trauma center, which can contribute to optimal resource use and indicate which type of surgical skills are necessary in our trauma emergency procedures.


Condition or disease Intervention/treatment
Trauma Injuries Other: Trauma team activation

  Show Detailed Description

Study Type : Observational [Patient Registry]
Actual Enrollment : 324 participants
Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration: 1 Month
Official Title: Evaluation of a University Hospital Trauma Team Activation Protocol: a Prospective Cohort Study
Study Start Date : February 2013
Actual Primary Completion Date : October 2016
Actual Study Completion Date : October 2016

Resource links provided by the National Library of Medicine


Group/Cohort Intervention/treatment
Seriously injured or potentially seriously injured patients Other: Trauma team activation
When admitting a potentially seriously injured patient, a trauma team is activated when prehospital information fulfills one or more prespecified criteria. The trauma team consist of a group of medical personnel including a surgeon, anesthesiologist and radiologist.




Primary Outcome Measures :
  1. Trauma team activation criteria [ Time Frame: 1 day ]
    The specific criterium or criteria that was fulfilled and was used to activate the trauma team


Secondary Outcome Measures :
  1. Emergency procedure [ Time Frame: 2 days ]
    All prespecified emergency procedures to stabilize airways, breathing and circulation will be registered.

  2. Mortality [ Time Frame: up to 30 days ]


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Ages Eligible for Study:   up to 100 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Severly injured and potentially severly injured patients admitted at the University Hospital North Norway
Criteria

Inclusion Criteria:

  • all patients admitted with the trauma team
  • all patients admitted with Injury Severity Score >15

Exclusion Criteria:

  • secondary admittance(transfers)>24 post injury

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01771861


Locations
Norway
University Hospital North Norway
Tromsø, Norway, 9036
Sponsors and Collaborators
University Hospital of North Norway

Responsible Party: University Hospital of North Norway
ClinicalTrials.gov Identifier: NCT01771861     History of Changes
Other Study ID Numbers: 2012/1912 (REK)
First Posted: January 18, 2013    Key Record Dates
Last Update Posted: October 28, 2016
Last Verified: October 2016

Additional relevant MeSH terms:
Wounds and Injuries