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Clinical Trials/NCT02165137
NCT02165137
Completed
Not Applicable

Quality Control in the Management of Major Trauma Patients at Aarau Cantonal Hospital - Evaluation of Processes and Patient Outcome

Kantonsspital Aarau1 site in 1 country3,800 target enrollmentJanuary 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Injury
Sponsor
Kantonsspital Aarau
Enrollment
3800
Locations
1
Primary Endpoint
emergency room process times
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Quality control and improvement project: Assessment and analysis of processes and outcome in trauma emergency room and major trauma patients at the Aarau trauma center (cantonal hospital) with regard to initial emergency management, hospital processes and short- and long-term (1-and 2-year) outcome of patients (subjective and objective). Comparison of processes and outcome pre- and post- project initiative. Benchmarking with the literature and by participation in the German and Swiss Trauma registry each.

Detailed Description

Registry of all emergency patients arriving at Aarau trauma center following trauma with regard to possibly injury related pre- and inhospital demographic factors, process variables and outcome Parameters.

Registry
clinicaltrials.gov
Start Date
January 2010
End Date
December 2020
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Kantonsspital Aarau
Responsible Party
Principal Investigator
Principal Investigator

Thomas Gross, MD

Prof. Dr. med.

Kantonsspital Aarau

Eligibility Criteria

Inclusion Criteria

  • major trauma: New Injury Severity Score (NISS) \>=8
  • for longer-term outcome: only patients firm in German language and able to respond to the postal questionnaire by themselves

Exclusion Criteria

  • no Trauma
  • injury \>24h before arrival at Aarau Cantonal Hospital
  • for longer-term outcome: patients not firm in German language and not able to respond to the postal questionnaire by themselves (dead, unavailable, refusal to participate, dementia, age\<16 years ecc.); a categorising compilation of cases is supposed to exclude any possible study bias

Outcomes

Primary Outcomes

emergency room process times

Time Frame: hours (<6)

Secondary Outcomes

  • Trauma Outcome Profile (TOP)(1 and 2 year follow-up)
  • Quality of Life after Brain Injury (QOLIBRI)(1 and 2 year follow-up)
  • Euro Quality of Life Group health-related quality of life on five dimensions (EQ-5D)(1 and 2 year follow-up)
  • hospital mortality(30 days)
  • medical outcomes study Short Form-36 (SF-36)(1 and 2 year follow-up)
  • reduced capacity to work(1 and 2 year outcome)

Study Sites (1)

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