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Selective CT for Anticoagulated Head Injured Patients

Head Injury | Traumatic Brain Injury | Intracranial Hemorrhage, Traumatic | Blunt Head Injury

The goal is to derive and a clinical decision rule for safe exclusion of traumatic brain injury without neuroimaging in head-injured ED patients who take anticoagulant medications.

The objectives are to:

1. Derive and externally validate a new highly sensitive and maximally specific clinical decision rule for the exclusion of traumatic brain injury in head-injured ED patients who take anticoagulant medications; and,
2. Estimate the sensitivity and specificity of existing head injury clinical decision rules in head-injured ED patients who take anticoagulant medications.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    16 and up

Participation Criteria

Inclusion Criteria:

* Age ≥16 years
* Presents to the emergency department after a head injury
* Patient has a head CT in the emergency department
* Is a current anticoagulant user

Exclusion Criteria:

* Head injury occurred \>48 h before patient's arrival to the emergency department
* Penetrating head injury
* Previously enrolled
* Patient resides outside of the hospital's catchment area
* Patient was transferred from another emergency department following neuroimaging
* Patient was not managed by the emergency or trauma physician in the emergency department
* Leaves the emergency department prior to completion of their medical assessment

Study Location

University of British Columbia
University of British Columbia
Vancouver, British Columbia
Canada

Contact Study Team

Primary Contact

David Barbic, MD

Sinai Health
Sinai Health
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Shelley McLeod, PhD, MSc

Ottawa Hospital Research Institute
Ottawa Hospital Research Institute
Ottawa, Ontario
Canada

Contact Study Team

Primary Contact

Gabriel Sandino-Gold

Hamilton Health Sciences Corporation
Hamilton Health Sciences Corporation
Hamilton, Ontario
Canada

Contact Study Team

Primary Contact

Natasha S Clayton, CRA, RA

[email protected]
Hôpital du Sacré-Cœur de Montréal
Hôpital du Sacré-Cœur de Montréal
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

Chantal Lanthier, RN

Kingston Health Sciences Centre
Kingston Health Sciences Centre
Kingston, Ontario
Canada

Contact Study Team

Primary Contact

Natasha S Clayton, CRA, RA

[email protected]
CHU de Québec - Université Laval
CHU de Québec - Université Laval
Québec City, Quebec
Canada

Contact Study Team

Primary Contact

Alexandra Nadeau

Study Sponsored By
Queen's University
Participants Required
More Information
Study ID: NCT05364749