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Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation — XXGA  

Medical Abortion Clinical Trial

Official title:
Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation: A Non-inferiority Trial

Clinical Trial Summary

To demonstrate non-inferiority of the efficacy of 200 mg mifepristone followed in 24 to 48 hours by 800 µg buccal misoprostol in outpatient medical abortion services among women 71-77 days' compared to women 64-70 days' LMP.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02314754
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase Phase 4
Start date December 2014
Completion date April 2016
View Details
See also
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