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Evaluation of Trauma Team Activation Criteria

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
University Hospital of North Norway
ClinicalTrials.gov Identifier:
NCT01771861
First received: January 16, 2013
Last updated: October 27, 2016
Last verified: October 2016
  Purpose

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 Intervention
Trauma Injuries Other: Trauma team activation

Study Type: Observational [Patient Registry]
Study Design: 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

Resource links provided by NLM:


Further study details as provided by University Hospital of North Norway:

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

  • Mortality [ Time Frame: up to 30 days ]

Enrollment: 324
Study Start Date: February 2013
Study Completion Date: October 2016
Primary Completion Date: October 2016 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
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.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   up to 100 Years   (Child, Adult, Senior)
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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01771861

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

Responsible Party: University Hospital of North Norway
ClinicalTrials.gov Identifier: NCT01771861     History of Changes
Other Study ID Numbers: 2012/1912 (REK)
Study First Received: January 16, 2013
Last Updated: October 27, 2016

Additional relevant MeSH terms:
Wounds and Injuries

ClinicalTrials.gov processed this record on June 23, 2017