Clarification of Optimal Anticoagulation Through Genetics

Brief Summary
Individuals taking warfarin often need frequent dose changes as the international normalized ratio (INR) gets too high or too low which could result in a higher risk of thromboembolism, bleeding and early discontinuation of a highly useful therapy. This study will compare two approaches to warfarin dosing to examine the utility of using genetic information for warfarin dosing.
Brief Title
Clarification of Optimal Anticoagulation Through Genetics
Detailed Description
The objective of the Clarification of Optimal Anticoagulation through Genetics (COAG) trial is to conduct a 1,022 participant, multicenter, double-blind, randomized trial comparing two approaches to guiding warfarin therapy initiation: 1) initiation of warfarin therapy based on algorithms using clinical information and an individual's genotype using genes known to influence warfarin response ("genotype-guided dosing"), and 2) initiation of warfarin therapy based on algorithms using only clinical information ("clinical-guided dosing"). The study hypothesis is that the use of genetic and clinical information for selecting the dose of warfarin during the initial dosing period will lead to improvement in stability of anticoagulation(AC) relative to a strategy that incorporates only clinical information (without genetics) for initial dosing. Each study arm will include a baseline dose initiation algorithm and a dose revision algorithm applied over the first 4 to 5 doses of warfarin therapy. By comparing the two strategies in this trial, the study will be able to determine if genetic information provides added benefit above and beyond what can be gleaned simply with clinical information. This study is a proof-of-concept efficacy trial. Efficacy is defined as a measure of whether, under optimal application, dosing algorithms will lead to improvement in care. The trial will thus answer the question: "can the use of clinical plus genetic information lead to an improvement in anticoagulation control above and beyond the use of only clinical information during the initiation of warfarin, when applied in a uniform and optimal manner to all patients?" Because efficacy has not yet been established for genotype-guided dosing of warfarin, it is important to first test whether this approach can, indeed, improve anticoagulation outcomes under controlled conditions.
Completion Date
Completion Date Type
Actual
Conditions
Stroke
Venous Thrombosis
Atrial Fibrillation
Atrial Flutter
Eligibility Criteria
Inclusion Criteria:

* Willingness and ability to sign informed consent
* Able to be followed in outpatient AC clinic
* Expected duration of warfarin therapy of at least 1 month
* AC management for the patient will be performed in-hospital and as an outpatient by clinicians that will adhere to the study dosing algorithms and dose titration plans
* Target INR 2-3

Exclusion Criteria:

* Currently taking warfarin
* Prior warfarin therapy with known required stable dose
* Clinician opinion that warfarin dosing needs to be adjusted for reasons not accounted for by dosing algorithm
* Abnormal baseline INR (off warfarin) (e.g., due to liver disease, antiphospholipid antibody)
* Contraindication to warfarin treatment for at least 3 months
* Life expectancy of less than 1 year
* Pregnant women or child-bearing women not using medically approved method of birth control (requires negative pregnancy test to exclude pregnancy in child-bearing women)
* Inability to follow-up on a regular basis with anticoagulation practitioners participating in the trial
* Any factors likely to limit adherence to warfarin
* Cognitive or other causes of inability to provide informed consent or follow study procedures
* Participating in another trial that prohibits participation in the COAG trial or planned enrollment in such a trial within the first 6 months of warfarin therapy
* Estimated blood loss of more than 1,000 cc requiring blood transfusions within 48 hours prior to randomization
* Genotype (CYP2C9 or VKORC1) known to participant from prior testing
Inclusion Criteria
Inclusion Criteria:

* Willingness and ability to sign informed consent
* Able to be followed in outpatient AC clinic
* Expected duration of warfarin therapy of at least 1 month
* AC management for the patient will be performed in-hospital and as an outpatient by clinicians that will adhere to the study dosing algorithms and dose titration plans
* Target INR 2-3

Gender
All
Gender Based
false
Keywords
Embolism
Thrombosis
Healthy Volunteers
No
Last Update Submit Date
Minimum Age
18 Years
NCT Id
NCT00839657
Org Class
Nih
Org Full Name
National Heart, Lung, and Blood Institute (NHLBI)
Org Study Id
623
Overall Status
Completed
Phases
Phase 3
Primary Completion Date
Primary Completion Date Type
Actual
Official Title
A Randomized, Multi-Center, Double-Blind Clinical Trial to Evaluate the Use of Clinical Plus Genetic Information to Guide Warfarin Therapy Initiation and Improve Anticoagulation Control for Patients
Primary Outcomes
Outcome Measure
Percentage of time participants spend within the therapeutic INR range (PTTR)
Outcome Time Frame
Measured during the first 4 weeks of therapy
Secondary Ids
Secondary Id
N01 HV88210
Secondary Id
HHSN268200800003C
Secondary Outcomes
Outcome Time Frame
Measured during the first 4 weeks
Outcome Measure
Occurrence of INR greater than 4 or serious clinical event
Start Date
Status Verified Date
First Submit Date
First Submit QC Date
Std Ages
Adult
Older Adult
Maximum Age Number (converted to Years and rounded down)
999
Minimum Age Number (converted to Years and rounded down)
18
Investigators
Investigator Type
Principal Investigator
Investigator Name
Henny Billett
Investigator Email
hbillett@montefiore.org
Investigator Phone
718-920-6310