Acceptability and Feasibility of a Simplified Medical Abortion Service Delivery in Western Ukraine

Abortion, Therapeutic Clinical Trial

Official title:
Acceptability and Feasibility of a Simplified Medical Abortion Service Delivery in Western Ukraine: A Demonstration Study of 800 mcg Buccal Misoprostol Following 200 mg Mifepristone for Abortion up to 70 Days Gestation

Status Completed

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

Abortion, Therapeutic

Clinical Trial Details

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

View Details

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