MedPath

Pharmacogenetic Dosing of Warfarin

Phase 3
Completed
Conditions
Stroke
Venous Thrombosis
Atrial Fibrillation
Atrial Flutter
Interventions
Behavioral: Standard of care dosing for warfarin
Genetic: Genotype-guided dosingTaiwan algorithm for warfarin
Genetic: Genotype-guided dosing IWPC algorithm for warfarin
Registration Number
NCT02065388
Lead Sponsor
Academia Sinica, Taiwan
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Patients must give their informed consent and complete the case report form.
  • Patients must be over the age of 20.
  • Patients have clinical indications for warfarin therapy but do not have any prior warfarin treatment.
Exclusion Criteria
  • Patients who did not complete the informed consent form or the CRF
  • Patients who are less than the age of 20.
  • 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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard of care dosing for warfarinStandard of care dosing for warfarinLoading dose (5mg) of warfarin for the first 3 days of treatment. Dose adjustment after initiation will using guideline modified from Tait el al. (1998).
Genotype-guided dosingTaiwan algorithm for warfarinGenotype-guided dosingTaiwan algorithm for warfarinInitial loading dosing of warfarin for the first 3 days of treatment will be determined by the Taiwan algorithm that uses clinical and genetic information. Dose adjustment after initiation will using guideline modified from Tait el al. (1998).
Genotype-guided dosing IWPC algorithm for warfarinGenotype-guided dosing IWPC algorithm for warfarinInitial loading dosing of warfarin for the first 3 days of treatment will be determined by the IWPC algorithm that uses clinical and genetic information. Dose adjustment after initiation will using guideline modified from Tait el al. (1998).
Primary Outcome Measures
NameTimeMethod
Time spent in target INR rangefirst 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.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Kaohsiung Medical University

🇨🇳

Kaohsiung, Taiwan

China Medical University Hospital

🇨🇳

Taichung, Taiwan

Chang Gung Memorial Hospital

🇨🇳

Taoyuan, Taiwan

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