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
| Type | Name | Description |
|---|---|---|
| DRUG | Clopidogrel | clopidogrel 300 mg on the day prior to angiography |
| DRUG | Clopidogrel | clopidogrel 600 mg on the day prior to angiography |
| DRUG | Clopidogrel | clopidogrel 300 mg followed by 75 mg daily started one week prior to angiography |
| DRUG | Clopidogrel | clopidogrel 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.