This trial is withdrawn!
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More info
You can access this
clinical trial
if you have
Acute Coronary Syndrome
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

The purpose of this study is to evaluate whether patients post PCI receiving clopidogrel who are carriers of at least one CYP 2C19 loss-of-function allele may achieve improved pharmacodynamic efficacy of clopidogrel when treated with the CYP 2C19 enzyme inducing agent, St. John's wort, as compared with placebo. Hypothesis 1. Reduced platelet reactivity is present in patients receiving St. John's wort as compared to placebo when utilized in combination with clopidogrel 2. The combination or St. John's wort and clopidogrel results in enhanced platelet inhibition

Provided treatments

  • Drug: Placebo
  • Drug: St. Johns Wort

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01330589. The sponsor of the trial is Lancaster General Hospital and it is looking for 0 volunteers for the current phase.
Official trial title:
The Effect of Inducing the Cytochrome P450 System on the Pharmacodynamic Efficacy of Clopidogrel