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This study is a blinded randomized trial to compare two different doses and intervals of buccal misoprostol for cervical preparation before surgical abortion at 13 to 16 weeks' gestation: 400 mcg admi...
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Lead Sponsor
Planned Parenthood of Greater New York
NCT00383032 · Abortion, Induced
NCT00188071 · Abortion, Induced
NCT01751087 · Abortion, Induced
NCT00855842 · Abortion, Induced
Planned Parenthood of New York City - Margaret Sanger Center
New York, New York
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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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