Clinical Trials Logo

Clinical Trial Summary

The study will examine how a simplified outpatient medical abortion procedure using mifepristone and misoprostol, with the option to take mifepristone at a place of woman's choosing, works in Ukraine. The investigators intend to demonstrate the efficacy of oral administration of 200 mg mifepristone and buccal administration of 800 mcg misoprostol with gestations through 70 days, as well as the acceptability of this method.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02981030
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase Phase 4
Start date November 23, 2016
Completion date June 30, 2017

See also
  Status Clinical Trial Phase
Recruiting NCT05182008 - A Patient Decision Aid for Method of Early Abortion: A Randomized Control Trial N/A
Completed NCT00310921 - A Randomized Study of Cervical Priming With Misoprostol Prior to Elective First Trimester Pregnancy Termination Phase 2
Completed NCT02037919 - Nexplanon Application Post-Abortion (NAPA) N/A