Warfarin Clinical Trial
Official title:
Randomized Controlled Trial of Patient Self-Testing of Warfarin Therapy Using an Internet Based Expert System
To test the hypothesis that home international normalised ratio (INR) monitoring with supervised patient self-testing (PST)can provide comparable or superior time in therapeutic range (TTR) to that provided by traditional outpatient anticoagulation.
Indications for anticoagulant treatment to prevent thromboembolic disease have increased in
recent years. INR must be monitored frequently to determine the safest dose and to minimize
the risk for thrombotic and haemorrhagic complications. Standard warfarin therapy is
associated with rates of major haemorrhage of up to 5-9% annually and recurrent venous
thromboembolism of up to 8%. These event rates are dependent of the model of care used to
manage warfarin therapy, with better outcomes associated with home testing of the INR which
enables patients to monitor their response to warfarin more frequently. INR results must
still be 'managed' by communicating the data to the healthcare provider, usually be
telephone or fax.
In this study we will evaluate a novel method of PST; supervised PST with an internet based
expert system, which 'manages' patients on oral anticoagulation by utilizing clinical and
laboratory data provided by the patient and dose adjustment and retesting algorithms derived
from clinical practice. Patients will be randomized to either 6 months of supervised PST or
routine medical care by the AMS. At the end of the 6 month period, each patient will then
'cross over' to the other management regimen and the difference in TTR between the two
periods will be compared.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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