Trial for new daily contraceptive pill withdrawn before starting
NCT ID NCT03296098
Summary
This study aimed to test a daily pill (ulipristal acetate) as a primary method to prevent pregnancy. It planned to enroll about 300 healthy women aged 18-35 to take the pill for six months. The main goals were to see how well it worked at preventing pregnancy and to check its safety and side effects, but the study was withdrawn before any participants were enrolled.
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Contacts and locations
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Locations
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Columbia University
New York, New York, 10032, United States
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Eastern Virginia Medical School (EVMS)
Norfolk, Virginia, 23507, United States
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Essential Access
Los Angeles, California, 90010, United States
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Johns Hopkins Bayview Medical Center
Baltimore, Maryland, 21224, United States
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New York University, School of Medicine
New York, New York, 10016, United States
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Oregon Health & Science University
Portland, Oregon, 97239, United States
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Planned Parenthood League of Massachusetts
Boston, Massachusetts, 02215, United States
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Univeristy of Pittsburgh School of Medicine
Pittsburgh, Pennsylvania, 15213, United States
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University Hospitals of Cleveland MacDonald Women's Hospital
Cleveland, Ohio, 44106, United States
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University of California, Davis
Sacramento, California, 95817, United States
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University of California, San Francisco
San Francisco, California, 94110, United States
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University of Chicago
Chicago, Illinois, 60637, United States
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University of Cincinnati
Cincinnati, Ohio, 45267, United States
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University of Colorado
Denver, Colorado, 80045, United States
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University of Hawaii
Honolulu, Hawaii, 96826, United States
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University of Pennsylvania Medical Center
Philadelphia, Pennsylvania, 19104, United States
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University of Utah
Salt Lake City, Utah, 84106, United States
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Women & Infants Hospital of Rhode Island
Providence, Rhode Island, 02905, United States
Conditions
Explore the condition pages connected to this study.