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Evaluation of the TICCS Capacity to Identify Trauma Patients With Acute Coagulopathy and Massive Bleeding

NCT02132208 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 82

Last updated 2014-05-07

No results posted yet for this study

Summary

A prospective single-centre non-comparative non-interventional open study has been designed to validate, in a target number of 100 trauma patients, the correlation between TICCS evaluated on the site of injury and thromboelastography made on a whole blood sample taken at the latest 30 min after patient's arrival in the resuscitation room.

The aim of this study was to evaluate the capacity to discriminate trauma patients suffering from active bleeding and arly acute coagulopathy of trauma and needing Damage control resuscitation from those without this aggravating combination with a new purely clinical easy-to-measure pre-hospital score: the Trauma Induced Coagulopathy Clinical Score (TICCS).

Conditions

  • Multiple Trauma
  • Massive Bleeding
  • Early Complication of Trauma

Sponsors & Collaborators

  • Centre Hospitalier Régional de la Citadelle

    lead OTHER

Principal Investigators

  • Martin L Tonglet, MD · CHR de la Citadelle, Liège, Belgium

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • Belgium

Study Locations

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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 NCT02132208 on ClinicalTrials.gov