Induced Abortion Clinical Trial
Official title:
An Open Label Study of 400 mcg Sublingual Misoprostol Following Mifepristone 200 mg for Abortion up to 63 Days LMP
This open-label study is being conducted to determine whether national expansion of a 400
mcg of sublingual misoprostol (i.e., under the tongue) taken 24 hours following
administration of mifepristone 200 mg is effective and acceptable to new abortion providers
in 14 regions.
The goal of this study is to provide answers to the following four questions:
1. What is the effectiveness of this regimen of medical abortion with mifepristone
followed by 400 mcg sublingual misoprostol up to 63 days since the last menstrual
period (LMP)?
2. Are the side effects with sublingual use tolerable for women?
3. Is sublingual administration of misoprostol acceptable to women?
4. Are women satisfied with counseling and services received in new centers offering
medical abortion?
n/a
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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