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Clinical Trial Summary

This open-label, comparative study will compare the efficacy, safety, and acceptability of 200 mg mifepristone followed in 24-48 hours by 800mcg buccal misoprostol or 400mcg sublingual misoprostol for termination of pregnancy in existing outpatient early medical abortion services among women 57-63 days' versus 64-70 days' gestation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00997347
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase Phase 4
Start date July 2009
Completion date February 2012

See also
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