Clinical Trials Directory

Trials / Completed

CompletedNCT00693069

Effect of Different Dosing Regimens of Clopidogrel Before Elective Percutaneous Coronary Intervention (PCI) on Platelet Function

Effect of Different Dosing Regimens of Clopidogrel Given Before Elective Percutaneous Coronary Intervention on Platelet Function

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Adequate platelet inhibition before percutaneous coronary intervention (PCI) reduces peri-procedural and long-term ischemic complications. Documented reduced response to clopidogrel has been associated with subsequent major adverse cardiovascular events. Strategies to optimize platelet inhibition pre-PCI are under investigation. This study sought to evaluate the effect on platelet aggregation of four different dosing regimens of clopidogrel given before elective PCI.

Conditions

Interventions

TypeNameDescription
DRUGClopidogrelclopidogrel 300 mg on the day prior to angiography
DRUGClopidogrelclopidogrel 600 mg on the day prior to angiography
DRUGClopidogrelclopidogrel 300 mg followed by 75 mg daily started one week prior to angiography
DRUGClopidogrelclopidogrel 300 mg followed by 150 mg daily started one week prior to angiography

Timeline

Start date
2004-09-01
Completion
2006-04-01
First posted
2008-06-06
Last updated
2012-08-21

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00693069. Inclusion in this directory is not an endorsement.