Skip to content

Randomized Controlled Feasibility Trial of the Fearon Algorithm to Improve Management of Unstable Warfarin

A Single-site, Randomized Controlled Feasibility Trial of the Fearon Algorithm to Improve Management of Patients With Unstable Warfarin Effect.

Status
Terminated
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02267408
Enrollment
42
Registered
2014-10-17
Start date
2014-11-30
Completion date
2017-02-03
Last updated
2018-04-06

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

Conditions

Hypoprothrombinemia

Keywords

Heart valve prosthesis, Anticoagulation, Warfarin

Brief summary

Patients on warfarin but with unstable international normalized ratio (INR) will be recruited to a randomized trial comparing dosing based on an algorithm (Fearon algorithm, named after the mathematician Michael Fearon), which uses historical data to estimate patients' sensitivity to warfarin and to dose changes as well as the lag time until a dose adjustment takes effect, or to the investigators standard management Main outcome is improvement in time in therapeutic range.

Detailed description

Patients with very variable INRs resulting in a low proportion of time in therapeutic range (TTR) have a higher risk of both bleeding complications and thromboembolic events. A good TTR is generally considered to be over 60% and excellent TTR is above 72% of time in range. The investigators will recruit patients with a TTR below 50%. The Fearon algorithm provides a more thorough understanding of the individual responses to changes in warfarin dose and with a personalized nomogram for dose adjustments and timing of laboratory tests the investigators have an opportunity to improve the TTR and on a larger scale to reduce clinically important adverse events. Before embarking on a large randomized trial with this revised Fearon algorithm-derived nomogram this pilot study with a randomized, open-label design will be performed to demonstrate proof of principle.

Interventions

OTHERWarfarin adjustment using the Fearon algorithm

All available historical data will be used to calculate with the Fearon algorithm the individual sensitivity to warfarin and to dose changes as well as lag time until a dose adjustment reaches full effect. Based on this a personal dosing nomogram will be developed and provided to the investigator and to the patients. This nomogram will be used during 6 month but override is possible if the investigator feels that the suggestion from the nomogram is unsafe.

OTHERWarfarin adjustment using standard dosing

Patients will receive warfarin dosing instructions from a trained nurse using fixed nomograms and computer-based dosing suggestion.

Sponsors

Epitome Pharmaceuticals
CollaboratorUNKNOWN
McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Dosing of warfarin according to the Fearon algorithm or routine during 6 months for patients with unstable INRs

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with mechanical heart valve prosthesis managed for the warfarin therapy by the Thrombosis Service at HHS-General Hospital. * Treated with warfarin for at least 1 year. * Therapeutic INR range 2.0-3.0 or 2.5-3.5. * TTR in the lowest quartile

Exclusion criteria

* Known poor compliance due to for example alcohol abuse or cognitive impairment * Refusal to provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Improvement in TTR6 monthsThe percent units of TTR during the 6 months will be compared with the percent units TTR in the previous year

Secondary

MeasureTime frameDescription
Proportion of patients with improvement in TTR6 monthsProportion of included patients with TTR improvement of more than 5 percent units

Countries

Canada

Outcome results

None listed

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