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To demonstrate non-inferiority of the efficacy of 200 mg mifepristone followed in 24 to 48 hours by 800 µg buccal misoprostol in outpatient medical abortion services among women 71-77 days' compared t...
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Lead Sponsor
Gynuity Health Projects
NCT07534982 · Retained Product of Conception After First Trimester Medical Abortion
NCT06708208 · Pregnancy, Violence Against Women (VAW), and more
NCT06795334 · Non-medical Abortion Surgery
NCT05119439 · Medical Abortion
NCT04941443 · Pain, Medical Abortion
Hartford GYN Center
Hartford, Connecticut
Atlanta Women's Center
Atlanta, Georgia
John H. Stroger, Jr. Hospital of Cook CountY
Chicago, Illinois
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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