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Prothrombin Times Outside the Therapeutic Range in Otherwise Stable Patients (FORESPEAK-0)

Primary Purpose

Atrial Fibrillation, Venous Thromboembolism, Ischemic Stroke

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
warfarin
warfarin
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring warfarin, dosing, prothrombin time, Heart valve prosthesis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients on long-term warfarin (for prophylaxis of arterial embolism in patients with atrial fibrillation or mechanical heart valve replacement, or secondary prophylaxis after VTE) with a target INR of 2.0-3.0 or 2.5-3.5,
  2. Anticoagulant therapy managed by the clinic (HHS - General Hospital) for at least 3 months prior to enrolment, and
  3. Maintenance dose of warfarin unchanged for the previous 3 months or longer.
  4. The INR result is outside the therapeutic range as follows:

For those with target 2.0-3.0: Either an INR of 1.5-1.9 or an INR of 3.1-4.4. For those with target 2.5-3.5: Either an INR of 1.5-2.4 or an INR of 3.6-4.4.

Exclusion Criteria:

  1. Age <18 years,
  2. Long-term (>1 week) change in any other medication
  3. Long-term (>1 week) change in diet, especially regarding green vegetables.
  4. Attending physician believes the patient is not suitable for the study (e.g. psychiatric disorder, history of non-compliance),
  5. Failure to obtain telephone consent.

Sites / Locations

  • Thrombosis Service, HHS-General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

No change

Change

Arm Description

Intervention Drug warfarin no change in the dose is performed

Intervention Drug Warfarin One dose increased if subtherapeutic level; one dose deleted or reduced if supratherapeutic level

Outcomes

Primary Outcome Measures

Number of Patients With Prothrombin Time Results Within the Therapeutic Range After 2 Weeks
The number of patients with "follow-up INRs" within the therapeutic range was compared for patients with a single dose skipped/reduced/added versus patients with no change of dose.

Secondary Outcome Measures

Full Information

First Posted
December 23, 2008
Last Updated
July 24, 2012
Sponsor
Hamilton Health Sciences Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00814177
Brief Title
Prothrombin Times Outside the Therapeutic Range in Otherwise Stable Patients
Acronym
FORESPEAK-0
Official Title
Management of Prothrombin Times Outside the Therapeutic Range in Patients on Warfarin and With Otherwise Stable Levels
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
January 2009 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hamilton Health Sciences Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Warfarin is very effective for the prevention of blood clots (thrombosis). A test of coagulation, the prothrombin time (PT) is used to monitor the effect. The PT response to warfarin can fluctuate as a result of interactions with a large number of other drugs, food or herbal agents as well as for no apparent reason. Thus, frequent monitoring of the PT and dose adjustments according to the results are required. One third of our patients remain on the same maintenance dose over 6 months. However, also these patients sometimes have a PT result moderately outside the therapeutic range without any obvious explanation. Too short PTs may be due to missed dose(s) or more dark green vegetables in the diet. Too long PTs may be due to a course of antibiotic therapy or less dark green vegetables. Laboratory errors may also occur and can cause deviations in any direction. Most likely, unnoticed fluctuations in the PT occur as well between the time points of monitoring. There are no guidelines on how to manage the treatment in this situation but there are some typical "behaviours". Behavior A: Some physicians simply let the patient continue with the same dose. "It is extremely unlikely that the very temporary dose adjustment has any effect on the PT result 4 weeks later and this is a "cosmetic procedure"." Behavior B: Others recommend the patients to take ½ - 1 additional dose in case of short PT and to skip a dose or take half dose in case of long PT, and thereafter to continue with the usual dose. "The investigators need to quickly correct the temporary aberration in order to avoid thrombotic or bleeding complications the next few days. This may seem like an issue of no importance. The investigators are however performing a series of studies to evaluate if these stable patients can be managed with blood tests less often than every 4 weeks. For that purpose it is important to know how often and why aberrant results occur, the implication and to what extent they can be ignored. The investigators hypothesis is that in patients with very stable PT-results and unchanged dose for 3 months, should continue with exactly the same maintenance dose, even when the result unexpectedly is slightly above or below the therapeutic range. The investigators believe that most of these occasional PT-results outside the therapeutic range are due to laboratory errors, perhaps missed doses by the patient or temporary change in diet or medications.
Detailed Description
Setting: Thrombosis Service at HHS - General Hospital. This center monitors the warfarin treatment for 1300 patients in the region. These patient regularly go to a laboratory where they live. Test results (INR-results) are faxed to the Thrombosis Service, which calls the patient the same day to inform them of the results, how to continue dosing the warfarin and when to go for the following blood test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Venous Thromboembolism, Ischemic Stroke, Myocardial Infarction
Keywords
warfarin, dosing, prothrombin time, Heart valve prosthesis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Actual)

8. Arms, Groups, and Interventions

Arm Title
No change
Arm Type
Experimental
Arm Description
Intervention Drug warfarin no change in the dose is performed
Arm Title
Change
Arm Type
Active Comparator
Arm Description
Intervention Drug Warfarin One dose increased if subtherapeutic level; one dose deleted or reduced if supratherapeutic level
Intervention Type
Drug
Intervention Name(s)
warfarin
Other Intervention Name(s)
Coumadin
Intervention Description
No change: Continue without any change in spite of prothrombin time outside the therapeutic range.
Intervention Type
Drug
Intervention Name(s)
warfarin
Other Intervention Name(s)
Coumadin
Intervention Description
Change: Increase one dose in case prothrombin time is below the therapeutic range; delete or reduce one dose in case prothrombin time is above the therapeutic range.
Primary Outcome Measure Information:
Title
Number of Patients With Prothrombin Time Results Within the Therapeutic Range After 2 Weeks
Description
The number of patients with "follow-up INRs" within the therapeutic range was compared for patients with a single dose skipped/reduced/added versus patients with no change of dose.
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients on long-term warfarin (for prophylaxis of arterial embolism in patients with atrial fibrillation or mechanical heart valve replacement, or secondary prophylaxis after VTE) with a target INR of 2.0-3.0 or 2.5-3.5, Anticoagulant therapy managed by the clinic (HHS - General Hospital) for at least 3 months prior to enrolment, and Maintenance dose of warfarin unchanged for the previous 3 months or longer. The INR result is outside the therapeutic range as follows: For those with target 2.0-3.0: Either an INR of 1.5-1.9 or an INR of 3.1-4.4. For those with target 2.5-3.5: Either an INR of 1.5-2.4 or an INR of 3.6-4.4. Exclusion Criteria: Age <18 years, Long-term (>1 week) change in any other medication Long-term (>1 week) change in diet, especially regarding green vegetables. Attending physician believes the patient is not suitable for the study (e.g. psychiatric disorder, history of non-compliance), Failure to obtain telephone consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sam Schulman, MD, PhD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thrombosis Service, HHS-General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
19640572
Citation
Schulman S, Melinyshyn A, Ennis D, Rudd-Scott L. Single-dose adjustment versus no adjustment of warfarin in stably anticoagulated patients with an occasional international normalized ratio (INR) out of range. Thromb Res. 2010 May;125(5):393-7. doi: 10.1016/j.thromres.2009.07.006. Epub 2009 Jul 29.
Results Reference
result

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Prothrombin Times Outside the Therapeutic Range in Otherwise Stable Patients

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