102
Participants
Start Date
January 31, 2013
Primary Completion Date
December 31, 2014
Study Completion Date
December 31, 2014
Misoprostol
The study group will receive two doses of misoprostol (200mcg each tablet) vaginal 12 and 4 hours prior insertion. After 24 hours of the insertion failure the women will return to the clinic and a new attempt of insertion will be done. At this time we will evaluate if the insertion was able to do or not.
Family Planning Clinic, University of Campinas, Campinas
University of Campinas, Campinas
Luis Bahamondes
OTHER