25-Year Experience With Polytraumatized Patients in a Level 1 Trauma Center

Sponsor
Medical University of Vienna (Other)
Overall Status
Completed
CT.gov ID
NCT04723992
Collaborator
(none)
1,400
1
325
4.3

Study Details

Study Description

Brief Summary

In this study patients who were admitted to our hospital with critical injuries were enrolled retrospectively from January 1992 to December 2019. 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.

Condition or Disease Intervention/Treatment Phase
  • Other: retrospective analysis

Study Design

Study Type:
Observational
Actual Enrollment :
1400 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
25-Year Experience With Polytraumatized Patients in a Level 1 Trauma Center.: Polytrauma Between 1995 and 2019: What Has Changed
Study Start Date :
Jan 1, 1992
Actual Primary Completion Date :
Jan 31, 2019
Actual Study Completion Date :
Jan 31, 2019

Outcome Measures

Primary Outcome Measures

  1. In-hospital mortality in polytrauma patients. [January 1st 1992 to December 31st 2019]

  2. Possible prognostic factors influencing the outcome of polytrauma patients. [January 1st 1992 to December 31st 2019]

    Evaluation of concomitant traumatic brain injury, resuscitation, injury severity and trauma mechanisms in polytrauma patients.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Vienna, Department of Traumatology Vienna Austria 1090

Sponsors and Collaborators

  • Medical University of Vienna

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Valerie Weihs, Dr. med. univ., Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT04723992
Other Study ID Numbers:
  • 1146/2020
First Posted:
Jan 26, 2021
Last Update Posted:
Jan 26, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 26, 2021