Trial Information
Summary: The purpose of this study is to determine if the study drug (an investigational blood-thinning medication) is as good as warfarin (Coumadin®) in reducing the formation of blood clots in the hearts of patients with atrial fibrillation.
This clinical research study is for adults 18 years and older
who have been diagnosed with atrial fibrillation (a type of
irregular heartbeat also known as an arrhythmia) and who need
treatment with blood-thinning medication because of an increased
risk of blood clotting.
All participants in the study will receive blood-thinning
medication; half will take warfarin (Coumadin®), while the other
half will take the investigational medication. Neither the study
team nor you will know which group you have been assigned - this is
known as a double-blind study. The group you are assigned to will
be determined at random by a computer, and not the study
doctor.
You will generally be required to visit the study site once a
month, but possibly more frequently when the study doctor considers
this necessary. It is anticipated that, for most study
participants, study duration will be around 2-3 years, but it could
be slightly more or less. The study team will explain the reasons
for this to you at your first visit.
All study related visits, exams and medication will be provided
at no cost. Compensation may be provided for study-related travel.
Participation is voluntary and you may withdraw from the study at
any time.
For more information, click this link:
www.AtrialFibrillationStudy.com/ctw3
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Contact:
Buffalo Cardiology & Pulmonary Associates, P.C.
6460 Main Street
Ventura, CA 93003
Telephone: 716-565-6403
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Trial listings updated: June 1, 2008 at 6:30:43 AM