Trial Information

Summary: Acute Coronary Syndrome

The primary objectives of this study are to see whether prasugrel can help people with a heart attack or symptoms associated with a threatened heart attack. Whether prasugrel is safe or has any side effects that might be associated with it and to see how prasugrel affects daily quality of life.

Study drug and study procedures will be made available to you at no cost.

To qualify, you must:

  • Be at least 18 years old

You will not qualify if you:

  • History of ischemic or hemorrhagic stroke
  • Females who are known to be pregnant, who have given birth within the past 90 days, or who are breastfeeding.
  • Currently receiving hemodialysis or peritoneal dialysis.
  • History of spontaneous gastrointestinal bleeding requiring in-hospital treatment
  • History of intolerance or allergy to aspirin

Contact:

Cinthi Pillai, Research Coordinator
Biomedical Research Alliance of New York
Jacobi Medical Center
1400 Pelham Pkwy South, Building 5 Room 230
Bronx, NY 10461
Email:

Profile Page: Biomedical Research Alliance of New York, Bronx, NY

If you would like to learn more about participating in this study, please send an e-mail message using the form below.

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Trial listings updated: June 1, 2008 at 6:44:46 AM


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