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Clinical Trial Summary

To test the hypothesis that a regimen of 200 mg oral mifepristone, with the option of home administration, followed by 800 μg buccal misoprostol 24 hours later for abortion through 70 days LMP will be feasible and acceptable in Singapore.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02985229
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase Phase 3
Start date October 2016
Completion date July 2017

See also
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