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Patient Self Testing of Warfarin Therapy

Randomized Controlled Trial of Patient Self-Testing of Warfarin Therapy Using an Internet Based Expert System

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00594828
Enrollment
163
Registered
2008-01-16
Start date
2006-07-31
Completion date
2008-04-30
Last updated
2008-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Warfarin

Keywords

Patient self-testing, Oral anticoagulation therapy, Expert Systems, Point-of-Care Systems, International Normalized Ratio

Brief summary

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.

Detailed description

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.

Interventions

DEVICECoaguChek (Patient self testing)

Patients will test their INR at home either biweekly, weekly or every 2 weeks using a CoaguChek point of care meter and communicate with the healthcare provider via an internet based expert system

DEVICEAnticoagulation Management Service (AMS)

Patients will attend the AMS for six months and have their INR checked every 4-6 weeks or more frequently, at the discretion of the clinician

Sponsors

Hoffmann-La Roche
CollaboratorINDUSTRY
Health Research Board, Ireland
CollaboratorOTHER
ZyCare Inc
CollaboratorINDUSTRY
University College Cork
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* on warfarin therapy for a minimum of 2 months * are expected to be on warfarin therapy for the duration of the 12 month study * internet access

Exclusion criteria

* inability to provide informed consent * inability to use a home INR meter * patients who do not have a telephone * more than 2 missed clinic appointments in the preceding 6 months * patients on anticoagulant drugs other than warfarin (eg heparin, low molecular weight heparin) * history of hemorrhagic complications with a therapeutic or therapeutic INR in the preceding 6 months * inability to attend the hospital at short notice, if necessary

Design outcomes

Primary

MeasureTime frame
The primary outcome variable used to assess therapeutic efficacy and safety will be the difference in TTR during the six months of AMS management and the six months of PST1 year

Secondary

MeasureTime frame
To compare the number of adverse events (haemorrhagic and thromboembolic) using PST and AMS management1 year

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026