Non-fatal Outcome After Trauma

NCT02508675 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 6500

Last updated 2018-03-29

No results posted yet for this study

Summary

The major aim of this project is to investigate the prevalence, recovery patterns and risk factors for health related quality of life functional, psychological, societal and economic outcome after trauma. Another aim is to validate the WHO Quality Of Life-bref (WHOQOL-Bref) questionnaire for the trauma population.

Conditions

Sponsors & Collaborators

  • Elisabeth-TweeSteden Ziekenhuis

    collaborator OTHER
  • Erasmus Medical Center

    collaborator OTHER
  • Tilburg University

    collaborator OTHER
  • Amphia Hospital

    collaborator OTHER
  • Catharina Ziekenhuis Eindhoven

    collaborator OTHER
  • Bravis Hospital

    collaborator OTHER
  • Elkerliek Hospital

    collaborator OTHER
  • Maas Hospital Pantein

    collaborator OTHER
  • St. Anna Ziekenhuis, Geldrop, Netherlands

    collaborator OTHER
  • Jeroen Bosch Ziekenhuis

    collaborator OTHER
  • Maxima Medical Center

    collaborator OTHER
  • Twee Steden Hospital

    collaborator UNKNOWN
  • Bernhoven Hospital

    collaborator OTHER
  • Maasstad Hospital

    collaborator OTHER
  • Network Emergency Care Brabant

    lead OTHER

Principal Investigators

  • Koen W Lansink, MD · St. Elisabeth Hospital, Tilburg, The Netherlands

  • Mariska A de Jongh, PhD · Network Emergency Care Brabant

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2018-07-31
Completion
2018-07-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02508675 on ClinicalTrials.gov