120
Participants
Start Date
March 31, 2006
Primary Completion Date
May 31, 2008
Study Completion Date
September 30, 2008
IUD insertion [Copper T-380A or Levonorgestrel (intrauterine system) IUS]
When a subject has chosen a method of intra-uterine contraception and has agreed to participate in the study, she will have the intra-uterine device of her choice inserted according to the Food and Druga Administration (FDA) instructions.
University of Utah, Salt Lake City
Boston Medical Center, Boston
University of Utah
OTHER
Boston University
OTHER