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临床试验/NCT02065388
NCT02065388已完成3 期

Pharmacogenetic Dosing of Warfarin

Academia Sinica, Taiwan6 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2009年9月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
300
试验地点
6
主要终点
Time spent in target INR range

研究概览

简要总结

Purpose:

Warfarin is now the most commonly used oral anticoagulant. This drug has inter-individual variability due to the genetic polymorphisms in the warfarin metabolizing enzyme, CYP2C9 and warfarin target, VKORC1. The investigators' team developed a pharmacogenetic dosing algorithm which can predict patients required warfarin dose, thus could prevent warfarin induced warfarin adverse events.

Methods:

The investigators recruited patients with indications for warfarin, the genotypes of VKORC1 and CYP2C9 were determined by the hospitals and verified by National Center for Genome Medicine. The investigators then randomized the patients to one of three arms: 1. Warfarin dose predicted by dosing algorithm developed by the International Warfarin pharmacogenetic Consortium (IWPC), 2. Algorithm developed by the Taiwan Warfarin Consortium and 3. Standard of care. The investigators aimed to determine whether using genetic dosing algorithm can lead to more stable dose and safer use of the drug.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

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

入选标准

  • Patients must give their informed consent and complete the case report form.
  • Patients must be over the age of
  • Patients have clinical indications for warfarin therapy but do not have any prior warfarin treatment.

排除标准

  • Patients who did not complete the informed consent form or the CRF
  • Patients who are less than the age of
  • Patients who had prior or is currently on warfarin treatment.
  • Patients who have hemorrhagic tendencies or hemorrhagic diseases defined as copious bleeding caused by viral or bacterial infections; cancer and hepatic dysfunction defined as GOP and GPT values three times higher than normal value
  • Patients who has Vitamin K deficiency
  • Female patients who is currently pregnant

结局指标

主要结局

Time spent in target INR range

时间窗: first month of therapy

time spent in target INR range Time in the target INR Range will be the primary endpoints because of its strong association with adverse events: patients with subtherapeutic INR values are at increased risk of thrombosis and patients with high INR values are at increased risk of hemorrhage during warfarin treatment initiation.

次要结局

未报告次要终点

研究者

发起方
Academia Sinica, Taiwan
申办方类型
Other
责任方
Sponsor

研究点 (6)

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