The AHEAD Study: Monitoring Anticoagulated Patients Who Suffer Head Injury

May 29, 2015 updated by: Professor Suzanne Mason, University of Sheffield
Existing practice in emergency departments (ED) in the United Kingdom (UK) for managing patients taking warfarin after a blunt head injury is variable with little research that supports the most appropriate way to manage these patients. The investigators aimed to undertake research in order to understand the range and frequency of outcomes following head injury in this group of patients and to develop robust clinical guidance for how they should be optimally managed in the future.

Study Overview

Status

Completed

Detailed Description

This prospective observational study aims to enrol patients taking warfarin that attend participating ED's (up to 33) in England and Scotland after blunt head injury. Over an 18-month period from Oct 2011, ED attendance data will be collected from each ED as well as information from patient questionnaires about the care the patient received and the status of their health 6-10 weeks after the injury. Patients who died due to their head injury, experienced surgery due to their injury, had a change identified on a CT scan or re-attended the ED with a clear head injury complication are defined as experiencing a poor outcome. Information such as the patients' conscious state (GCS), level of clotting in their blood (INR) and symptoms will be investigated as predictors of a poor outcome. A mathematical model will be used to estimate the most cost-effective strategy assuming published National Institute for Health and Care Excellence (NICE) thresholds for cost per quality adjusted life year (QALY).

Study Type

Observational

Enrollment (Actual)

3556

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adults who attend participating emergency departments (ED) with a head injury and also prescribed warfarin

Description

Inclusion Criteria:

  • 16 years or older
  • Blunt head trauma above the neck within 24 hours of ED attendance
  • Prescribed warfarin

Exclusion Criteria:

  • Penetrating injuries to the head, for example knife wound.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rate of head injury complication in study cohort
Time Frame: 18 months
Head injury complications defined as death or neurosurgery resulting from the initial injury, a clinically-significant CT scan finding or re-attendance to the ED with a significant head injury-related complication up to 10 weeks after the original attendance.
18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of ongoing symptoms relating to the head injury
Time Frame: 18 months
Impaired activities of daily living (assessed by the EQ5D)
18 months
Prevalence of ongoing symptoms relating to the head injury
Time Frame: 18 months
Headache symptoms
18 months
Prevalence of ongoing symptoms relating to the head injury
Time Frame: 18 months
Impaired cognitive function (assessed by the Glasgow Outcome Scale)
18 months
Identification of early predictors of adverse clinical outcome
Time Frame: 18 months
Including clinical features and initial investigations which may be useful as a diagnostic tool.
18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Suzanne Mason, MD, University of Sheffield

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2011

Primary Completion (Actual)

March 1, 2013

Study Completion (Actual)

March 1, 2013

Study Registration Dates

First Submitted

May 27, 2015

First Submitted That Met QC Criteria

May 29, 2015

First Posted (Estimate)

June 3, 2015

Study Record Updates

Last Update Posted (Estimate)

June 3, 2015

Last Update Submitted That Met QC Criteria

May 29, 2015

Last Verified

May 1, 2015

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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