Non-Interventional
OtherNon-Interventional
NCT Number: NCT03087474
In a population of patients with venous thromboembolism and treated with oral anticoagulants (OAC) in routine clinical practice in Denmark this study will describe patients treated with each OAC
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Notify Me18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Non-Interventional
Time frame: Approximately 180 months
Hospitalization rate for first-time Venous thromboembolism (VTE) in Vitamin K antagonist (VKA) patients
Time frame: Approximately 180 months
Time frame: Approximately 180 months
Time frame: Approximately 180 months
Hospitalization rate for first-time venous thromboembolism in nonvitamin K antagonist oral anticoagulants (NOAC) patients
Time frame: Approximately 180 months
Time frame: Approximately 180 months
Time frame: Approximately 180 months
Time frame: Approximately 180 months
Bristol-Myers Squibb
Industry
Treatment of Venous Thromboembolism in Real-Life Patients: A Nationwide, Population-Based Study
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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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