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临床试验/NCT04001166
NCT04001166已完成不适用

Pharmacogenomics of Antithrombotic Drugs (PreMed PGx Study)

VTT Technical Research Centre of Finland1 个研究点 分布在 1 个国家目标入组 7,005 人开始时间: 2019年10月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
7,005
试验地点
1
主要终点
Incidence of bleeding complications

研究概览

简要总结

This is a retrospective cohort study linking data from Finnish Biobanks (Helsinki Biobank, Auria Biobank and THL Biobank), laboratory databases, and national registries of Social Insurance Institution of Finland (Kela) and the National Institute of Health and Welfare (THL) to investigate pharmacogenomics of antithrombotic drugs in the Finnish population. The purpose of the study is to assess clinical and economic aspects of using genomic data in the context of antithrombotic drug therapy.

Based on earlier research, data regarding variant alleles in CYP2C9 and VKORC1 will be used in the primary analyses. Individuals with and without specific variant alleles are compared in respect to their clinical response to warfarin therapy. Warfarin-treated individuals are also analysed in relation to other clinical outcomes and a wide range of healthcare encounters.

The explorative part of the study will employ data-driven classification methods to explore genotype-phenotype associations for a larger group of antithrombotic drugs including direct oral anticoagulants, clopidogrel and heparins and possible interactions with other drugs. In this part, 26 gene variants identified in literature will be used.

The retrospective follow-up time for the study participants is from January 2007 to December 2018, or 2 years prior the first anticoagulant drug is purchased until 6 months after the last purchase.

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
是

入选标准

  • •Genotyped for CYP2C9/rs1799853, CYP2C9/rs1057910 and VKORC1/rs9923231
  • •Diagnosed with at least one of the following:
  • •Atrial Fibrillation and Flutter (I48)
  • •Ischemic Heart Disease (I20-I25)
  • •Cerebrovascular disease (I63,I65,I66, 167.2, I69.3-I69.8)
  • •Atherosclerosis (I70)
  • •Pulmonary embolism (I26)
  • •Phlebitis and thrombophlebitis (I80)
  • •Portal vein thrombosis (I81)
  • •Other venous embolism and thrombosis (I82)
  • •Purchased at least one of the following drugs between January 1st 2007 - December 31st 2018:
  • •Anticoagulants: Warfarin, Dabigatran, Apixaban, Rivaroxaban, Edoxaban, Heparin, Enoxaparin, Dalteparin
  • •Antiplatelets: Clopidogrel, Ticagrelor, Acetylsalicylic acid

排除标准

  • •Permanent residence in Finland less than 12 months during the follow-up period
  • •Purchase of any of the antithrombotic drugs listed above between January 1st 2005 - December 31st 2006

结局指标

主要结局

Incidence of bleeding complications

时间窗: During warfarin treatment and beyond 6 months after the treatment

Incidence of bleeding complications in warfarin-treated individuals

次要结局

  • The number of hospital inpatient days(During warfarin treatment and beyond 6 months after the treatment)
  • Incidence of outpatients visits(During warfarin treatment and beyond 6 months after the treatment)
  • Time-weighted mean INR(During warfarin treatment and beyond 6 months after the treatment)
  • Incidence of emergency room (ER) visits(During warfarin treatment and beyond 6 months after the treatment)
  • Indicidence of hospital admissions(During warfarin treatment and beyond 6 months after the treatment)
  • The number of laboratory tests(During warfarin treatment and beyond 6 months after the treatment)
  • Incidence of medical procedures(During warfarin treatment and beyond 6 months after the treatment)
  • Time in Therapeutic Range (TTR)(During warfarin treatment and beyond 6 months after the treatment)
  • Time to reach therapeutic range(During warfarin treatment and beyond 6 months after the treatment)
  • Incidence of laboratory visits(During warfarin treatment and beyond 6 months after the treatment)

研究者

发起方
VTT Technical Research Centre of Finland
申办方类型
Other
责任方
Sponsor

研究点 (1)

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