The AHEAD Study: Monitoring Anticoagulated Patients Who Suffer Head Injury

NCT ID: NCT02461498

Last Updated: 2015-06-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

3556 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-07-31

Study Completion Date

2013-03-31

Brief Summary

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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.

Detailed Description

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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).

Conditions

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Craniocerebral Trauma Head Injuries, Closed

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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.
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute for Health Research, United Kingdom

OTHER_GOV

Sponsor Role collaborator

University of Sheffield

OTHER

Sponsor Role lead

Responsible Party

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Professor Suzanne Mason

Professor of Emergency Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Suzanne Mason, MD

Role: PRINCIPAL_INVESTIGATOR

University of Sheffield

References

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Mason S, Kuczawski M, Teare MD, Stevenson M, Goodacre S, Ramlakhan S, Morris F, Rothwell J. AHEAD Study: an observational study of the management of anticoagulated patients who suffer head injury. BMJ Open. 2017 Jan 13;7(1):e014324. doi: 10.1136/bmjopen-2016-014324.

Reference Type DERIVED
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Kuczawski M, Stevenson M, Goodacre S, Teare MD, Ramlakhan S, Morris F, Mason S. Should all anticoagulated patients with head injury receive a CT scan? Decision-analysis modelling of an observational cohort. BMJ Open. 2016 Dec 13;6(12):e013742. doi: 10.1136/bmjopen-2016-013742.

Reference Type DERIVED
PMID: 27974370 (View on PubMed)

Other Identifiers

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PB-PG-0808-17148

Identifier Type: -

Identifier Source: org_study_id

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