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Completed

NCT Number: NCT00830570

The Clinical and Economic Impact of Pharmacogenomic Testing of Warfarin Therapy in Typical Community Practice Settings

The purpose of this quasi-experiment study, which could also be classified as a prospective observational intervention study, is to assess the impact of cytochrome P450 2C9 (CYP 2C9) and vitamin K epoxide reductase complex, subunit 1 (VKORC1) testing within a primary patient care setting.

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Key information

Age range

40 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Medco Health Solutions, Inc.

Franklin Lakes, New Jersey, 07003, United States

About this study

Anticoagulation therapy with warfarin is the most common mode of treatment and prophylaxis for venous and arterial thromboembolic conditions. Warfarin is metabolized in the liver by the cytochrome P450 system, the cytochrome P450 2C9 (CYP 2C9) isoenzyme specifically, and polymorphisms in the CYP 2C9 gene have been associated with changes in metabolic function of the translated isoenzyme . These polymorphisms result in reduced metabolism of warfarin as compared to subjects having the wild type gene, consequently leading to systemic accumulation of warfarin; it is theorized that this leads to higher risk of adverse events. Other allelic variations have also been linked to changes in vitamin K conservation through their effects on vitamin K epoxide reductase complex, subunit 1 (VKORC1) . The combined impact of CYP 2C9 and VKORC1 polymorphisms on warfarin's pharmacology have recently been reported.

It is hypothesized that evaluation of genomic allelic type guided warfarin dosing will reduce thromboembolic and bleeding risks associated with warfarin therapy, and that adoption of a genetic testing strategy in a primary patient care setting would improve warfarin effectiveness and patient safety, and reduce costs to health care payers.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female and male age range of 40-75
  • Patients who are in the induction phase of warfarin
  • Patients receiving warfarin to prevent or treat thromboembolic conditions (e.g., post orthopedic surgery prophylaxis, deep venous thrombosis, atrial fibrillation, pulmonary embolism, heart failure)
  • Patient willing to provide informed consent prior to the specimen collection procedure
  • Patient whose physician is willing to order the genetic test

Exclusion criteria

  • Age < 40 or > 75
  • Previous use of warfarin within 180 days of initiating new warfarin therapy
  • Hospitalized for seven or more days before first claim for warfarin
  • Previous history of genetic testing for warfarin therapy
  • Known hypersensitivity to warfarin
  • Patient or physician refusal to participate in the study
  • Patients using warfarin residing in Olmsted County, MN

Treatment and study plan

CYP 2C9 and VKORC1 Testing for Warfarin

Other

Test patients for their warfarin sensitivity and provide this information to their physician authorizing the test.

Other names: Genetic testing for drug sensitivity

Primary outcomes

  1. The primary objective of the study is to determine whether the addition of genotyping to usual care will reduce the hospitalization rates for hemorrhage or thromboembolism related to warfarin use during the first 6 months of treatment.

    Time frame: 6 months

Secondary outcomes

  1. The secondary objective is to determine physician and patient acceptance of the technology.

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Medco Health Solutions, Inc.

Industry

Collaborators

  • Mayo Clinic
  • Washington University School of Medicine

Registry information

Official study title

in Typical Community Practice Settings

Acronym: MHSMayoWarf1

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Jan 28, 2009
Registry last updated
Nov 16, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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