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This open-label, randomized study is being conducted to determine whether a dose of 400 mcg of sublingual misoprostol (i.e., under the tongue) taken 24 hours following administration of mifepristone 2...
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Lead Sponsor
Gynuity Health Projects
NCT06894732 · Induced Abortion
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NCT00324519 · Pregnancy Trimester, Second, Induced Abortion
State University of Medicine and Pharmacy
Chisinau
Centre de Planification Familiale de l'Ariana
Aryanah
Centre de Planification Familiale la Bardo
Tunis
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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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