Red Blood Cell Distribution Width and Charlson Comorbidity Indeces in the Frail Polytraumatized Patient.

Sponsor
Medical University of Vienna (Other)
Overall Status
Completed
CT.gov ID
NCT05221476
Collaborator
(none)
400
47

Study Details

Study Description

Brief 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. RDW values on admission as well as preexisting comorbidities were evaluated.

Condition or Disease Intervention/Treatment Phase
  • Other: retrospective

Study Design

Study Type:
Observational
Actual Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
RDW and CCI in the Frail Polytraumatized Patients. A Retrospective Cohort Study in a Level 1 Trauma Center.
Actual Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
polytraumatized patients

Patients with an ISS >16 points, an AIS >3 in one body region and at least 2 different body regions affected were included.

Other: retrospective
The investigators retrospectively analyzed the short- and long-term outcome in polytraumatized patients and the possible influence of RDW values on admission as well as preexisting comorbidities on these outcomes.

Outcome Measures

Primary Outcome Measures

  1. In-hospital mortality in polytraumatized patients [January 2012 to December 2015]

Secondary Outcome Measures

  1. Possible influence of RDW values (%) on admission on the long-term outcome [January 2012 to December 2015]

    The influence of RDW Values (%) in polytraumatized patients on admission on the long-term outcome (late-phase death (days)) will be examined.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

No locations specified.

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, MD, Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT05221476
Other Study ID Numbers:
  • RDW Polytrauma
First Posted:
Feb 3, 2022
Last Update Posted:
Feb 3, 2022
Last Verified:
Jan 1, 2022
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 Feb 3, 2022