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临床试验/NCT02657616
NCT02657616已完成不适用

Stroke Prophylaxis of Patients With Atrial Fibrillation: Real-life Effectiveness and Safety of Novel Anticoagulants Compared to Vitamin-k-antagonists Based on an Analysis of German Claims Data

Institut für Pharmakoökonomie und Arzneimittellogistik e.V.0 个研究点目标入组 204,464 人开始时间: 2015年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
204,464
主要终点
Death

研究概览

简要总结

The central questions of the study can be summarized as follows:

What stroke / death rates are the result of the use of the following treatment strategies: no anticoagulation with vitamin-k-antagonists (VKAs) or novel oral anticoagulants (NOACs), anticoagulation with VKAs and anticoagulation with NOACs (all). What other thromboembolic complication rates resulting from the use of these treatment strategies? What heavy bleeding rates resulting from the defined management strategies? The analysis is based on a data set of patients with atrial fibrillation (AF)(01/01/2010 - 30/06/2014). 2010 is used as the reference period and 01/01/2011-30/06/2013 as the inclusion period. The minimum observation time per patient is 12 months.

Used is a data base of the AOK PLUS as well as the AOK Baden-Württemberg and AOK Bayern.

The aim of the study is to compare clinical outcomes between the different treatment strategies (frequency of events and time to first event). The influence of alternative treatment strategies is measured on the basis of three different methodological approaches: unadjusted comparison of event council and time to first event between the defined patient groups; matched-pair comparison (propensity score matching) between the different groups of patients (treatment strategies) and multivariate analysis using time to event (Cox proportional hazards model) as the dependent variable.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • one inpatient or two outpatient confirmed diagnosis of atrial fibrillation in two different quarters
  • Continuously insured by the AOK PLUS, AOK Bayern or AOK Baden-Württemberg

排除标准

  • Age < 18 years
  • Maximum possible observational period < 12 months (exception: death)

研究组 & 干预措施

Anticoagulation with vitamin-k-antagonists

The patient should be treated stable during the observation period with vitamin-k-antagonists (at least one prescription per half-year). The patient should be not been around on other anticoagulants during the observation period. This means that no prescriptions of novel anticoagulants and not more than 30 days should be observable prescriptions of low molecular weight heparins/Clopidogrel per year.

干预措施: vitamin-k-antagonists (Drug)

Anticoagulation with novel oral anticoagulants

The patient should be treated stable during the observation period with a novel anticoagulant (at least one prescription per half-year). This means that no vitamin-k-antagonists prescriptions and not more than 30 days should be observable prescriptions of low molecular weight heparins/Clopidogrel per year from the start of the observation period.

干预措施: Novel oral anticoagulants (Drug)

结局指标

主要结局

Death

时间窗: 01/01/2011-30/06/2014; at least 12 months; up to 40 months

Transient ischemic attack

时间窗: 01/01/2011-30/06/2014; at least 12 months; up to 40 months

Ischemic stroke

时间窗: 01/01/2011-30/06/2014; at least 12 months; up to 40 months

Hemorrhagic stroke

时间窗: 01/01/2011-30/06/2014; at least 12 months; up to 40 months

Heavy bleeding

时间窗: 01/01/2011-30/06/2014; at least 12 months; up to 40 months

次要结局

未报告次要终点

研究者

发起方
Institut für Pharmakoökonomie und Arzneimittellogistik e.V.
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sabrina Müller

Principal investigator

Institut für Pharmakoökonomie und Arzneimittellogistik e.V.

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