A Multicenter Study to Evaluate the Effects of a 91-Day Extended Cycle Oral Contraceptive on Hemostatic Parameters in Healthy Women



Status:Archived
Conditions:Women's Studies
Therapuetic Areas:Reproductive
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:November 2010
End Date:November 2011

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A Multinational, Multicenter, Randomized, Open-Label Study to Evaluate the Impact of a 91-Day Extended Cycle Oral Contraceptive Regimen, Compared to Two 28-day Standard Oral Contraceptive Regimens, on Hemostatic Parameters in Healthy Women.


This study is being conducted to evaluate the impact of a 91-day extended cycle oral
contraceptive compared to two 28-day oral contraceptive regimens on hemostatic parameters in
healthy women.



We found this trial at
13
sites
Uniontown, Pennsylvania 15401
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Uniontown, PA
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Albuquerque, New Mexico 87102
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Albuquerque, NM
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Arlington, Virginia 22203
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Arlington, VA
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Clearwater, Florida 33759
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Clearwater, FL
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Fort Collins, Colorado 80524
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Fort Collins, CO
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Houston, Texas 77054
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Houston, TX
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La Mesa, California 91942
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La Mesa, CA
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Lawrence, New Jersey 08648
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Lawrence, NJ
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Port Jefferson, New York 11777
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Port Jefferson, NY
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Savannah, Georgia 31406
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Savannah, GA
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Seattle, Washington 98105
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Seattle, WA
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Washington, Washington DC 20036
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Washington, DC
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Winston-Salem, North Carolina 27103
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Winston-Salem, NC
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