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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04335838
Other study ID # 1816/2016
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2012
Est. completion date December 2015

Study information

Verified date April 2020
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study patients who were admitted to our hospital with critical injuries were enrolled retrospectively from January 2012 to December 2015. Patients with an ISS>16 points, an AIS >3 in one body region and at least 2 different body regions affected were included. Possible prognostic factors were evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ISS >16 points

- AIS >3 in one body region

- at least 2 body regions affected

Exclusion Criteria:

- patients younger than 18 years of age

- isolated traumatic brain injury

- minor injuries (AIS <3 or ISS <16 points)

Study Design


Intervention

Other:
retrospective analysis
The investigators retrospectively analyzed the outcome and possible prognostic factors in polytrauma patients.

Locations

Country Name City State
Austria Medical University of Vienna, Department of Traumatology Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary In-hospital mortality in polytrauma patients. January 1, 2012 to December 31, 2015
Secondary Possible prognostic factors influencing the outcome of polytrauma patients. Evaluation of concomitant traumatic brain injury, resuscitation, injury severity and trauma mechanisms in polytrauma patients. Januar 1, 2012 to December 31, 2015
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