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Clinical Trial Summary

This study seeks to evaluate the efficacy, side effect profile and acceptability of a medical abortion regimen with mifepristone and two doses of 800 mcg misoprostol buccally at 71-77 and 78-84 days of gestation to further expand the evidence base for the most effective regimens in the late first trimester of pregnancy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05119439
Study type Interventional
Source Gynuity Health Projects
Contact
Status Terminated
Phase Phase 4
Start date October 7, 2022
Completion date June 30, 2023

See also
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