Clinical Trials Directory

Trials / Completed

CompletedNCT00670943

Effect of Abrupt Plavix® Discontinuation on Platelet Function

Status
Completed
Phase
Study type
Observational
Enrollment
52 (estimated)
Sponsor
Université de Montréal · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The well established importance of regular administration of antiplatelet drugs stands on firm grounds, as large meta-analyses have shown these therapies to significantly reduce the risk of death. Plavix® (clopidogrel) is widely used following coronary angioplasty, to reduce the risk of periprocedural thrombotic complications, for up to one year. As the current recommendations suggest clopidogrel use for no longer than one year, the drug is normally discontinued within that period. In the limited state of knowledge on antiplatelet drug withdrawal, an early sound of alarm has risen from early thromboembolic complications reported after the interruption of antiplatelet treatment used in prevention of ischemic vascular disease. Although little information is available, discontinuation of thienopyridines has been associated with increased thromboembolic complications, mainly acute stent thrombosis. These complications may signal a platelet sensitization effect to aggregating stimuli by antiplatelet drugs taken chronically. The current study aims to evaluate the impact of clopidogrel discontinuation on platelet function, in order to shed light on underlying mechanisms leading to increased risk of acute thrombo-occlusive events.

Conditions

Interventions

TypeNameDescription
OTHERPlatelet function testing

Timeline

Start date
2008-01-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2008-05-02
Last updated
2009-03-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00670943. Inclusion in this directory is not an endorsement.

Effect of Abrupt Plavix® Discontinuation on Platelet Function (NCT00670943) · Clinical Trials Directory