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OpenTrials
Completed

NCT Number: NCT02996851

Traumatic Intracranial Hemorrhage in Users of Oral Antithrombotic Drugs

Oral antithrombotic medications (OAM) are used for the prevention and treatment of thrombotic disorders. Among hemorrhagic complications of OAMs, intracranial hemorrhage (ICH) may have particularly devastating consequences with high morbidity, disability and mortality rates. The efficacy and safety profiles of OAMs are generally assessed in randomized controlled trials (RCT), but included patients are often highly selected and may not be representative of users in everyday clinical practice in terms of follow-up routines, age, gender, drug compliance, and polypharmacy. Moreover, it is often unclear whether or not traumatic ICHs are registered and reported in RCTs. Drifts in indications and treatment criteria may also be seen in everyday practice and drug discontinuation due to precautionary concerns including compliance, fall risk and comorbidity may be forgotten. Collectively, these factors may lead to other and potentially higher traumatic ICH rates in general clinical use than reported in RCTs.

The incidence rates of traumatic ICH in patients on OAMs in the general population remain unknown. In this nationwide registry based pharmacoepidemiological study we will investigate the incidence and case fatality of traumatic ICH in users of OAMs in Norway from 2008 through 2014.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • included in the Norwegian patient registry (NPR) and/or the Norwegian prescription database (NorPD)

Exclusion criteria

-

Treatment and study plan

Primary outcomes

  1. incidence of intracranial hemorrhage requiring hospital admission

    Time frame: at least 12 months following intracranial hemorrhage

    Age- and gender-adjusted comparisons of annual incidence rates will be carried out

Secondary outcomes

  1. incidence of fatal traumatic intercranial hemorrhage defined as death within 90 days of admission

    Time frame: 90 days

    Age- and gender-adjusted comparisons of annual incidence rates will be carried out.

  2. overall survival following traumatic intracranial hemorrhage

    Time frame: 6 years

Sponsors and collaborators

Lead sponsor

St. Olavs Hospital

Other

Collaborators

  • Norwegian University of Science and Technology

Registry information

Official study title

Traumatic Intracranial Hemorrhage in Users of Oral Antithrombotic Drugs: a Nationwide Pharmacoepidemiological Study

Important dates

Study start
2007
Primary completion
2014
Study completion
2014
First posted
Dec 19, 2016
Registry last updated
Oct 17, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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