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Optimising thromboembolic and stroke prevention in pharmacist-managed oral anticoagulotherapy

Completed
Conditions
Circulatory System
Stroke
Thromboembolism and stroke
Registration Number
ISRCTN76463647
Lead Sponsor
Cité de la Santé de Laval (Canada)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
500
Inclusion Criteria

1. The patient is referred to the Pharmacy Managed Anticoagulation Service (PMAS) with a prescription of warfarin for at least six months
2. The patient is aged 18 years and older, either sex
3. The patient agrees to go to the Cité de la Santé de Laval, the Centre Hospitalier Ambulatoire Régional de Laval, or one of the four Laval Centre Local de Services Communautaire for blood drawing during participation in the study (six months)
4. The patient lives in the Laval area
5. The patient is able to read and speak French or English
6. The patient agrees to participate in the study and has signed the informed consent form
7. The patient's treating physician has agreed to participate and has signed the informed consent form
8. It is expected that the patient will be transferred to the treating physician

Exclusion Criteria

1. The patient participates to another study
2. The patient is referred to the PMAS for a pre-admission

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The percentage of time spent within the target INR range.
Secondary Outcome Measures
NameTimeMethod
1. Incidence and severity of major thromboembolic and haemorrhagic events<br>2. Health-related quality of life<br>3. Direct medical-care costs
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